Grandfathering Provisions of the Medicare DMEPOS Competitive Bidding Program

ICR 201608-0938-007

OMB: 0938-1079

Federal Form Document

ICR Details
0938-1079 201608-0938-007
Historical Active 201306-0938-004
HHS/CMS CMS-10309
Grandfathering Provisions of the Medicare DMEPOS Competitive Bidding Program
Revision of a currently approved collection   No
Regular
Approved with change 02/17/2017
Retrieve Notice of Action (NOA) 08/11/2016
  Inventory as of this Action Requested Previously Approved
02/29/2020 36 Months From Approved 02/28/2017
110,250 0 654,464
13,605 0 79,799
0 0 0

We established the grandfathering process in the April 10, 2007 final rule for competitive bidding (72 FR 17992) for rented DME and oxygen and oxygen equipment when these items are included under the Medicare DMEPOS Competitive Bidding Program. This process only applies to suppliers that rented DME and oxygen and oxygen equipment to beneficiaries who maintain a permanent residence in a CBA before the implementation of the competitive bidding program. We established beneficiary notification requirements for noncontract suppliers that are furnishing rented oxygen or DME competitive bid items at the time a competitive bidding program is implemented in a competitive bidding area (74 FR 61738). This notification will ensure that beneficiaries are sufficiently informed and prepared for competitive bidding changes that affect rented DME and oxygen.

PL: Pub.L. 108 - 173 302(b)(1) Name of Law: Competitive Acquisition
  
None

Not associated with rulemaking

  81 FR 18855 04/01/2016
81 FR 46925 07/19/2016
No

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 110,250 654,464 0 -544,214 0 0
Annual Time Burden (Hours) 13,605 79,799 0 -66,194 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
Yes
Cutting Redundancy
The burden associated with this ICR is decreasing and adjusted by annualizing the one-time burden estimates. For this approval period, the burden estimates have been updated by removing the estimates that were related to Round 2 and updating the estimates for the implementation of Round 1 2017. The burden estimates to develop and send the 30-day notification to beneficiaries for Round 1 has changed from the previous version because we estimate that there will be more beneficiaries who reside in a CBA and will be renting DME and oxygen competitively bid items at the start of Round 1 2017. This increases the time required to develop and send the notification. Additionally, the cost to the supplier to develop and send the notifications has increased as the median hourly wage for clerical staff has increased according to the May 2014 data from the Bureau of Labor Statistics.

$0
No
No
No
No
No
Uncollected
Kayla Williams 410 786-5887 Kayla.Williams@cms.hhs.gov

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
08/11/2016


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