Osteonics PS Hemi-Hip Stem Series

FDA 510(k) K933882 · Osteonics Corp.

Substantially Equivalent for Some Indications

510(k) numberK933882

Submission

Device name
Osteonics PS Hemi-Hip Stem Series
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
August 10, 1993
Decision date
August 14, 1995
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3358
Specialty
Orthopedic
Implant
Yes

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More from Encore Medical L.P.

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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 Osteonics PS Hemi-Hip Stem Series cleared by the FDA?

Osteonics PS Hemi-Hip Stem Series (K933882) received a 510(k) decision of Substantially Equivalent for Some Indications on August 14, 1995, 734 days after the submission was received.

What is the product code of K933882?

The FDA product code is LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3358.