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Sigma 96-1240A

by Depuy Orthopaedics, Inc.

Sigma 96-1240A (961240A) is a Class I device made by Depuy Orthopaedics, Inc., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 10603295236245), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10603295236245 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Sigma
Generic name
Knee tibia prosthesis trial, reusable
Model / Ref / Catalog
96-1240A, 961240A
Primary DI / UDI-DI
10603295236245
FDA product code
HWT
GMDN term
Knee tibia prosthesis trial, reusable
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Category: Knee tibia prosthesis trial, reusable

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)