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

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

22 pages