Mod-Ml Unicompartmental Knee Prosthesis

FDA 510(k) K896856 · Osteonics Corp.

Substantially Equivalent for Some Indications

510(k) numberK896856

Submission

Device name
Mod-Ml Unicompartmental Knee Prosthesis
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
December 5, 1989
Decision date
February 6, 1990
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HSX – Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3520
Specialty
Orthopedic
Implant
Yes

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K251771Cambridge Partial KneeHSX · Traditional Signature Orthopaedics Pty, Ltd.12/16/2025SE
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K251453Arthrex iBalance Partial Knee SystemHSX · Traditional Arthrex, Inc.07/01/2025SE
K241260ACTIFY™ Unicondylar Knee SystemHSX · Traditional Globus Medical, Inc.12/06/2024SE
K242711JOURNEY II Unicompartmental Knee System (JOURNEY II UK)HSX · Traditional Smith & Nephew, Inc.10/30/2024SE
K242746OvertureTi Knee Resurfacing SystemTMHSX · Special Overture Orthopaedics10/07/2024SE
K232114TRIBRID® Unicompartmental Knee SystemHSX · Traditional Kyocera Medical Technologies, Inc.04/04/2024SE

More from Kyocera Medical Technologies, Inc.

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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 Mod-Ml Unicompartmental Knee Prosthesis cleared by the FDA?

Mod-Ml Unicompartmental Knee Prosthesis (K896856) received a 510(k) decision of Substantially Equivalent for Some Indications on February 6, 1990, 63 days after the submission was received.

What is the product code of K896856?

The FDA product code is HSX – Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3520.