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FDA 510(k) K884888, MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS, by Protek, Inc.

FDA 510(k) K884888, MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS, by Protek, Inc.

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510(K) Number: K884888
Device Name: MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
Manufacturer: Protek, Inc.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, cemented
Regulation Number: 888.3350
Classification Product Code: JDI
Date Received: 11/22/1988
Decision Date: 12/29/1988
Regulation Medical Specialty: Orthopedic

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