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Accolade 6058-0335D

by Howmedica Osteonics Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number07613327020748 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Accolade
Generic name
Uncoated hip femur prosthesis, modular
Model / Ref / Catalog
6058-0335D
Primary DI / UDI-DI
07613327020748
FDA product code
LPH, MBL, MEH, JDI, MAY, KWL, KWZ, LWJ, LZO, KWY
GMDN term
Uncoated hip femur prosthesis, modular
Device class
Class II
Regulation number
888.3358, 888.3353, 888.3350, 888.3360, 888.3310, 888.3390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Uncoated hip femur prosthesis, modular

Other devices from Howmedica Osteonics Corp.

See all devices from Howmedica Osteonics Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number

Other properties (10)

  • Sterilise before use: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No