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Anthology AFIT 71935579

by Smith & Nephew, 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 Number00885556686508 UDI-DI Date6 Nov 2017ListedStatusListed 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  • Withdrawn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
Anthology AFIT
Generic Name
Coated hip femur prosthesis, modular
Model / Ref / Catalog
71935579
Primary DI / UDI-DI
00885556686508
510(k) Number
FDA Product Code
LPH
GMDN Term
Coated hip femur prosthesis, modular
Device Class
Class II
Regulation Number
888.3358
GUDID distribution status
In Commercial Distribution

Related devices

Category: Coated hip femur prosthesis, modularCoated femoral stem prosthesis, modular

Cleared under the same submission (K172684)

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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