FDA PMA FDA Class 2 Approved 🇺🇸 United States

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

PMA: P850061 · Supplement: S001 · Decision Mar 29, 1989
Classifications
1
FEI Numbers
271
Registration Numbers
271

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Trade Name
BIAS(R) FIBER METAL TOTAL HIP SYSTEM
PMA Number
P850061
Supplement Number
S001
Device Class
FDA Class 2
Product Code
LPH
Generic Name
PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
Regulation Number
888.3358
Medical Specialty
Orthopedic
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
March 29, 1989
Date Received
February 8, 1989
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented