Omnifit Ceramic Morse Taper Head

FDA 510(k) K894694 · Osteonics Corp.

Substantially Equivalent

510(k) numberK894694

Submission

Device name
Omnifit Ceramic Morse Taper Head
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
July 24, 1989
Decision date
October 12, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LZO – Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3353
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code LZO

510(k)DeviceApplicantDecision
K253948Momentum Acetabular Cup SystemLZO · Traditional United Orthopedic Corporation09/02/2026SE
K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)LZO · Traditional Waldemar Link GmbH & Co. KG07/06/2026SE
K260831Z1 Hip SystemLZO · Traditional Zimmer, Inc.06/16/2026SE
K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemLZO · Traditional Zimmer, Inc.04/27/2026SE
K260037implantcast Packaging System UpdateLZO · Traditional Implantcast GmbH03/30/2026SE
K252401implaFit® short stemsLZO · Traditional Implantcast GmbH03/12/2026SE
K253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)LZO · Traditional Maxx Orthopedics, Inc.01/15/2026SE
K250450Coated hip implantsLZO · Traditional Medacta International S.A.09/19/2025SE
K243021Longboard Revision Hip StemLZO · Traditional Signature Orthopaedics Pty, Ltd.08/07/2025SE
K251906Z1 Hip SystemLZO · Special Zimmer, Inc.07/18/2025SE

More from Zimmer, Inc.

510(k)DeviceDecision
K983657Osteonics Series 7000 Ad Tibial TrayHRY · Traditional 04/06/2000SE
K980070Osteonics Ha-Coated DevicesMEH · Traditional 07/23/1999SE
K984375Osteonics Spinal System - Sacral Offset Connector AssemblyKWP · Traditional 04/30/1999SE
K982798Osteonics Anterior Cervical Compression Plating SystemKWQ · Traditional 03/25/1999SE
K984585Osteonics +10 Unipolar Adaptor SleeveKWL · Traditional 02/24/1999SE
K990203Osteonics Primary Secur-Fit Plus Hip StemsMEH · Special 02/18/1999SE
K990158Osteonics Combination Screw Ring/BlockerMNI · Special 02/01/1999SE
K984302Osteonics Spinal System Cylindrical Bone ScrewsMNH · Special 12/18/1998SE
K984353Osteo 9MM Ic Tibial NailHSB · Special 12/16/1998SE
K983502Osteonics Secur-Fit Ad Generation II Acetabular Component SystemLPH · Traditional 12/16/1998SE

Questions and answers

When was Omnifit Ceramic Morse Taper Head cleared by the FDA?

Omnifit Ceramic Morse Taper Head (K894694) received a 510(k) decision of Substantially Equivalent on October 12, 1989, 80 days after the submission was received.

What is the product code of K894694?

The FDA product code is LZO – Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3353.