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Revision Knee System 2471-0-0001

by Consensus Orthopedics, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number00844588014642 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Revision Knee System
Generic Name
Revision coated hip femur prosthesis
Model / Ref / Catalog
2471-0-0001
Primary DI / UDI-DI
00844588014642
FDA Product Code
JWH
GMDN Term
Revision coated hip femur prosthesis
Device Class
Class II
Regulation Number
888.3560
GUDID distribution status
Not in Commercial Distribution

Other devices from Consensus Orthopedics, Inc.

See all devices from Consensus Orthopedics, Inc. →

Properties

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

Other properties (7)

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