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Klassic Knee Template, Tibial Baseplate, Revision 2909.00.000

by Total Joint Orthopedics, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810094692674 UDI-DIDate7 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Klassic Knee Template, Tibial Baseplate, Revision
Generic Name
Surgical implant template, reusable
Model / Reference
2909.00.000
Primary DI / UDI-DI
00810094692674
FDA Product Code
HWT
GMDN Term
Surgical implant template, reusable
Device Class
Class I
Regulation Number
888.4800
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription Use

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No