FDA 510(k), K921277, RANAWAT/BURSTEIN TOTAL HIP SYSTEM

FDA 510(k), K921277, RANAWAT/BURSTEIN TOTAL HIP SYSTEM

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510(K) Number: K921277
Device Name: RANAWAT/BURSTEIN TOTAL HIP SYSTEM
Manufacturer: PATRICIA BERES
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation Number: LPH
Classification Product Code: KXA
Date Received: 03/17/1992
Decision Date: 02/16/1994
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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