Skip to content

Scp® 514153

by Zimmer Knee Creations, Inc.

Scp® 514153 is a Class I device made by Zimmer Knee Creations, Inc., listed in FDA GUDID since 3 Jul 2025 (UDI-DI 00889024686953), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024686953 UDI-DI Date3 Jul 2025ListedStatusListed 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  • Withdrawn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
Scp®
Generic name
Bone graft delivery kit
Model / reference
514153
Primary DI / UDI-DI
00889024686953
FDA product code
OJH
GMDN term
Bone graft delivery kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone graft delivery kit

Similar devices

Other devices filed under FDA product code OJH (Orthopedic Tray).

Other devices from Zimmer Knee Creations, Inc.

See all devices from Zimmer Knee Creations, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)