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Self Centering 1037-40-000

by Depuy Orthopaedics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295003533 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Self Centering
Generic Name
Bipolar femoral head outer component, hemiarthroplasty
Model / Ref / Catalog
1037-40-000, 103740000
Primary DI / UDI-DI
10603295003533
510(k) Number
FDA Product Code
KWY
GMDN Term
Bipolar femoral head outer component, hemiarthroplasty
Device Class
Class II
Regulation Number
888.3390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bipolar femoral head outer component, hemiarthroplasty

Cleared under the same submission (K812672)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No