Pca +15MM Modular Femoral Head

FDA 510(k) K955305 · Howmedica Corp.

Substantially Equivalent

510(k) numberK955305

Submission

Device name
Pca +15MM Modular Femoral Head
Applicant
Howmedica Corp.
Rutherford, NJ, US
Received
November 20, 1995
Decision date
January 18, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

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K983528Micro Dynamic MeshJEY · Traditional 12/23/1998SE
K983404Type 3 Femoral ComponentsLZO · Traditional 12/22/1998SE
K980926Duration II Acetabular Components-Ethylene Oxide SterilizationJDI · Traditional 12/16/1998SE
K980925Duration II Tibial Inserts-Ethylene Oxide SterilizationJWH · Traditional 12/16/1998SE
K980632Duration II Tibial Inserts - Gas Plasma SterilizationJWH · Traditional 12/11/1998SE
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Questions and answers

When was Pca +15MM Modular Femoral Head cleared by the FDA?

Pca +15MM Modular Femoral Head (K955305) received a 510(k) decision of Substantially Equivalent on January 18, 1996, 59 days after the submission was received.

What is the product code of K955305?

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