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MUTARS® femoral stem cementless 57600515

by implantcast GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048844049812 UDI-DI Date5 Apr 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MUTARS® femoral stem cementless
Generic Name
Press-fit hip femur prosthesis, modular
Model / Reference
57600515
Primary DI / UDI-DI
04048844049812
510(k) Number
FDA Product Code
LZO
GMDN Term
Press-fit hip femur prosthesis, modular
Device Class
Class II
Regulation Number
888.3353
GUDID distribution status
In Commercial Distribution

Related devices

Category: Press-fit hip femur prosthesis, modular

Cleared under the same submission (K181778)

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