Medicare Program; Establishment of Special Payment Provisions and Requirements for Qualified Practitioners and Qualified Suppliers of Prosthetics and Custom-Fabricated Orthotics; Withdrawal, 46181-46182 [2017-21425]
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Federal Register / Vol. 82, No. 191 / Wednesday, October 4, 2017 / Proposed Rules
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3302–WN]
42 CFR Part 416, 418, 482, 483, and 485
Medicare and Medicaid Programs;
Revisions to Certain Patient’s Rights
Conditions for Participation and
Conditions for Coverage; Withdrawal
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Withdrawal of proposed rule.
AGENCY:
This document withdraws a
proposed rule that was published in the
Federal Register on December 12, 2014.
This proposed rule would revise the
applicable conditions of participation
for certain providers, conditions for
coverage for certain suppliers, and
requirements for long-term care
facilities, to ensure that the
requirements are consistent with the
Supreme Court decision in United
States v. Windsor (570 U.S.12, 133 S. Ct.
2675 (2013)), and HHS policy.
Specifically, it proposed to revise
certain definitions and patient’s rights
provisions that currently defer to state
law, in order to ensure that same-sex
spouses are recognized and afforded
equal rights in certain Medicare and
Medicaid-participating facilities.
DATES: As of October 4, 2017, the
proposed rule published December 12,
2014, at 79 FR 73873, is withdrawn.
FOR FURTHER INFORMATION CONTACT:
Ronisha Blackstone, 410–786–6882.
SUPPLEMENTARY INFORMATION: On
December 12, 2014, we published a
proposed rule in the Federal Register
entitled, ‘‘Medicare and Medicaid
Program; Revisions to Certain Patient’s
Rights Conditions of Participation and
Conditions for Coverage’’ (79 FR 73873).
In United States v. Windsor, 570 U.S.12,
133 S. Ct. 2675 (2013), the Supreme
Court held that section 3 of the Defense
of Marriage Act (DOMA) was
unconstitutional because it violated the
Fifth Amendment (See Windsor, 133 S.
Ct. 2675, 2695). Section 3 of DOMA
provided that in determining the
meaning of any Act of the Congress, or
of any ruling, regulation, or
interpretation of the various
administrative bureaus and agencies of
the United States, the word ‘‘marriage’’
meant only a legal union between one
man and one woman as husband and
wife, and the word ‘‘spouse’’ could refer
only to a person of the opposite sex who
was a husband or a wife (1 U.S.C. 7).
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Following the Supreme Court’s opinion
in Windsor, the Federal government was
permitted to recognize the validity of
same-sex marriages when administering
Federal statutes and programs.
The December 2014 rulemaking
proposed to revise certain conditions of
participation (CoPs), conditions for
coverage (CfCs), and requirements for
certain Medicare- and Medicaidparticipating facilities to ensure that the
requirements at issue were consistent
with the Windsor decision. We received
97 public comments in response to the
December 2014 proposed rule.
Following publication of the proposed
rule, on June 26, 2015 in Obergefell v.
Hodges, (135 S. Ct. 2584 (2015)), the
Supreme Court held that the Due
Process and Equal Protection clauses of
the Fourteenth Amendment requires a
state to license a marriage between two
people of the same sex, and to recognize
same-sex marriages lawfully performed
in other States. In light of the Obergefell
decision, we have decided to withdraw
the December 2014 proposed rule. We
believe that the Obergefell decision has
addressed many of the concerns raised
in the December 2014 proposed rule.
Accordingly, the proposed rule
published December 12, 2014, at 79 FR
73873, is withdrawn.
Dated: August 24, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Approved: September 7, 2017.
Thomas E. Price,
Secretary, Department of Health and Human
Services.
[FR Doc. 2017–21419 Filed 10–3–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 424
[CMS–6012–WN]
RIN 0938–AR84
Medicare Program; Establishment of
Special Payment Provisions and
Requirements for Qualified
Practitioners and Qualified Suppliers
of Prosthetics and Custom-Fabricated
Orthotics; Withdrawal
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Withdrawal of proposed rule.
AGENCY:
Federal Register on January 12, 2017.
The proposed rule specified the
qualifications needed for qualified
practitioners to furnish and fabricate,
and qualified suppliers to fabricate
prosthetics and custom-fabricated
orthotics; accreditation requirements
that qualified suppliers must meet in
order to bill for prosthetics and custom
fabricated orthotics; requirements that
an organization must meet in order to
accredit qualified suppliers to bill for
prosthetics and custom-fabricated
orthotics; and a timeframe by which
qualified practitioners and qualified
suppliers must meet the applicable
licensure, certification, and
accreditation requirements. In addition,
the proposed rule removed the current
exemption from accreditation and
quality standards for certain
practitioners and suppliers.
As of October 4, 2017, the
proposed rule published January 12,
2017, at 82 FR 3678, is withdrawn.
DATES:
FOR FURTHER INFORMATION CONTACT:
In the
January 12, 2017 Federal Register (82
FR 3678), we published a proposed rule
titled, ‘‘Medicare Program;
Establishment of Special Payment
Provisions and Requirements for
Qualified Practitioners and Qualified
Suppliers of Prosthetics and Custom
Fabricated Orthotics’’ to ensure that
only those who are qualified to do so
can furnish, fabricate, and bill for the
prosthetics and custom-fabricated
orthotics addressed by the proposed
rule.
We received over 5,000 public
comments in response to the January 12,
2017 proposed rule.
In light of the cost and time burdens
that the proposed rule would create for
many providers and suppliers,
particularly the cost and burden for
those providers and suppliers that are
small businesses, and the complexity of
the issues raised in the detailed public
comments received, we are withdrawing
the January 12, 2017 proposed rule in
order to assure agency flexibility in reexamining the issues and exploring
options and alternatives with
stakeholders.
Accordingly, the proposed rule
published January 12, 2017, at 82 FR
3678, is withdrawn.
SUPPLEMENTARY INFORMATION:
This document withdraws a
proposed rule that was published in the
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John
Spiegel, (410) 786–1909.
SUMMARY:
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46181
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Federal Register / Vol. 82, No. 191 / Wednesday, October 4, 2017 / Proposed Rules
Dated: July 21, 2017.
Demetrios L. Kouzoukas,
Principal Deputy Administrator and Director,
Center for Medicare.
Approved: September 7, 2017.
Thomas E. Price,
Secretary, Department of Health and Human
Services.
[FR Doc. 2017–21425 Filed 10–3–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
42 CFR Part 511
[CMS–1670–WN]
RIN 0938–AS85
Medicare Program; Part B Drug
Payment Model; Withdrawal
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Withdrawal of proposed rule.
AGENCY:
This document withdraws a
proposed rule that was published in the
Federal Register on March 11, 2016.
The proposed rule discussed our
proposal to implement a new Medicare
payment model under section 1115A of
the Social Security Act (the Act).
DATES: As of October 4, 2017, the
proposed rule published March 11,
2016, at 81 FR 13230, is withdrawn.
FOR FURTHER INFORMATION CONTACT:
Rasheeda Johnson, (410) 786–3434.
SUPPLEMENTARY INFORMATION: On March
11, 2016, we published a proposed rule
in the Federal Register entitled
‘‘Medicare Program; Part B Drug
Payment Model’’ (81 FR 13230). The
rule proposed the Part B Drug Payment
Model as a two-phase model that would
test whether alternative drug payment
designs will lead to a reduction in
Medicare expenditures, while
preserving or enhancing the quality of
care provided to Medicare beneficiaries.
In the first phase, CMS would test a
change to the 6 percent add-on to
Average Sales Price (ASP) that is used
to make drug payments under Part B
such that the add-on would be 2.5
percent plus a flat fee (in a budget
neutral manner). In the second phase,
we would implement a collection of
value-based purchasing tools similar to
those employed by commercial health
plans, pharmacy benefit managers,
hospitals, and other entities that manage
health benefits and drug utilization. We
proposed to operate the model for 5
years; phase I would begin in the fall of
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SUMMARY:
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2016 (no earlier than 60 days after the
rule was finalized), and phase II would
begin no sooner than January 1, 2017.
The proposed goal was to have both
phases of the model in full operation
during the last 3 years of the proposed
5-year duration to fully evaluate
changes and collect sufficient data.
We received 1,350 timely public
comments in response to the March 11,
2016, proposed rule. Some commenters
signaled their support for the proposed
rule, however, a number of commenters
expressed concerns about the proposed
model. As we worked to address these
concerns, the complexity of the issues
related to the proposed model design
and the desire to increase stakeholder
input led us to the decision to withdraw
the March 11, 2016 proposed rule.
Moving forward, we want to ensure
agency flexibility in re-examining these
important issues and exploring new
options and alternatives with
stakeholders as we develop potential
payment models that support innovative
approaches to improve quality,
accessibility, and affordability, reduce
Medicare program expenditures, and
empower patients and doctors to make
decisions about their health care.
Accordingly, the proposed rule
published March 11, 2016, at 81 FR
13230, is withdrawn.
Dated: July 17, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: August 25, 2017.
Thomas E. Price,
Secretary, Department of Health and Human
Services.
[FR Doc. 2017–21420 Filed 10–3–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
45 CFR Parts 160 and 162
[CMS–0037–WN]
Administrative Simplification:
Certification of Compliance for Health
Plans; Withdrawal
Office of the Secretary, HHS.
ACTION: Withdrawal of proposed rule.
AGENCY:
This document withdraws the
January 2, 2014, proposed rule that
would have required a controlling
health plan (CHP) to submit information
and documentation demonstrating that
it is compliant with certain standards
and operating rules adopted by the
SUMMARY:
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Secretary of Health and Human Services
(the Secretary) under the Health
Insurance Portability and
Accountability Act of 1996 (HIPAA).
This proposed rule would have also
established penalty fees for a CHP that
failed to comply with the certification of
compliance requirements.
As of October 4, 2017, the
proposed rule published January 2,
2014, at 79 FR 298, is withdrawn.
DATES:
FOR FURTHER INFORMATION CONTACT:
Geanelle G. Herring, (410) 786–4466.
In the
January 2, 2014, Federal Register (79 FR
298), we published the proposed rule
titled ‘‘Administrative Simplification:
Certification of Compliance for Health
Plans’’ which would have required
controlling health plans (CHPs) to
submit certain information and
documentation that demonstrated
compliance with the standards and
operating rules adopted under the
Health Insurance Portability and
Accountability Act of 1996 (HIPAA) for
three electronic transactions: Eligibility
for a health plan, health care claim
status, and health care electronic funds
transfers (EFT) and remittance advice.
The proposed rule would have also
established penalty fees for a CHP that
failed to comply with the certification of
compliance requirements.
We received approximately 72 public
comments in response to the January 2,
2014 proposed rule. In light of the
issues raised in the public comments
received, we have decided to withdraw
the January 2014 proposed rule in order
to re-examine the issues and explore
options and alternatives to comply with
the statutory requirements. We note that
the Secretary has established regulations
pertaining to compliance with, and
enforcement of, HIPAA Administrative
Simplification standards and operating
rules. The withdrawal of this proposed
rule does not remove the requirements
for covered entities to comply with any
of those regulations codified at 45 CFR
parts 160 and 162.
Accordingly, the proposed rule
published January 2, 2014, at 79 FR 298,
is withdrawn.
SUPPLEMENTARY INFORMATION:
Dated: August 18, 2017.
Seema Verma,
Administrator, Centers for Medicare &
Medicaid Services.
Dated: August 30, 2017.
Thomas E. Price,
Secretary, Department of Health and Human
Services.
[FR Doc. 2017–21424 Filed 10–3–17; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\04OCP1.SGM
04OCP1
Agencies
[Federal Register Volume 82, Number 191 (Wednesday, October 4, 2017)]
[Proposed Rules]
[Pages 46181-46182]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-21425]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 424
[CMS-6012-WN]
RIN 0938-AR84
Medicare Program; Establishment of Special Payment Provisions and
Requirements for Qualified Practitioners and Qualified Suppliers of
Prosthetics and Custom-Fabricated Orthotics; Withdrawal
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Withdrawal of proposed rule.
-----------------------------------------------------------------------
SUMMARY: This document withdraws a proposed rule that was published in
the Federal Register on January 12, 2017. The proposed rule specified
the qualifications needed for qualified practitioners to furnish and
fabricate, and qualified suppliers to fabricate prosthetics and custom-
fabricated orthotics; accreditation requirements that qualified
suppliers must meet in order to bill for prosthetics and custom
fabricated orthotics; requirements that an organization must meet in
order to accredit qualified suppliers to bill for prosthetics and
custom-fabricated orthotics; and a timeframe by which qualified
practitioners and qualified suppliers must meet the applicable
licensure, certification, and accreditation requirements. In addition,
the proposed rule removed the current exemption from accreditation and
quality standards for certain practitioners and suppliers.
DATES: As of October 4, 2017, the proposed rule published January 12,
2017, at 82 FR 3678, is withdrawn.
FOR FURTHER INFORMATION CONTACT: John Spiegel, (410) 786-1909.
SUPPLEMENTARY INFORMATION: In the January 12, 2017 Federal Register (82
FR 3678), we published a proposed rule titled, ``Medicare Program;
Establishment of Special Payment Provisions and Requirements for
Qualified Practitioners and Qualified Suppliers of Prosthetics and
Custom Fabricated Orthotics'' to ensure that only those who are
qualified to do so can furnish, fabricate, and bill for the prosthetics
and custom-fabricated orthotics addressed by the proposed rule.
We received over 5,000 public comments in response to the January
12, 2017 proposed rule.
In light of the cost and time burdens that the proposed rule would
create for many providers and suppliers, particularly the cost and
burden for those providers and suppliers that are small businesses, and
the complexity of the issues raised in the detailed public comments
received, we are withdrawing the January 12, 2017 proposed rule in
order to assure agency flexibility in re-examining the issues and
exploring options and alternatives with stakeholders.
Accordingly, the proposed rule published January 12, 2017, at 82 FR
3678, is withdrawn.
[[Page 46182]]
Dated: July 21, 2017.
Demetrios L. Kouzoukas,
Principal Deputy Administrator and Director, Center for Medicare.
Approved: September 7, 2017.
Thomas E. Price,
Secretary, Department of Health and Human Services.
[FR Doc. 2017-21425 Filed 10-3-17; 8:45 am]
BILLING CODE 4120-01-P