FDA PMA FDA Class 3 Approved 🇺🇸 United States

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic, Cemented

PMA: P820024 · Supplement: S009 · Decision Jan 21, 1987
Classifications
1
FEI Numbers
1
Registration Numbers
1

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic, Cemented
Trade Name
PROSTHESIS, HIP, HEMI-FEMORAL, METAL
PMA Number
P820024
Supplement Number
S009
Device Class
FDA Class 3
Product Code
LPF
Generic Name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic, cemented
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
January 21, 1987
Date Received
December 12, 1986
Supplement Type
Normal 180 Day Track
Supplement Reason
Other
Expedited Review
N

Classifications

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

Product Code Device Name
LPF Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic, Cemented