FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P000013 · Supplement: S004 · Decision Aug 16, 2004
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
Trade Name
OSTEONICS ABC/TRIDENT SYSTEMS
PMA Number
P000013
Supplement Number
S004
Device Class
FDA Class 3
Product Code
MRA
Generic Name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
August 16, 2004
Date Received
April 15, 2004
Supplement Type
Real-Time Process
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE TRIDENT "T" SHELL FOR USE WITH THE TRIDENT ALUMINA INSERT. THE TRIDENT "T" SHELL, WHICH FEATURES A THICKER SHELL WALL, IS A LINE EXTENSION TO THE TRIDENT ACETABULAR SHELLS PREVIOUSLY APPROVED FOR USE WITH THE TRIDENT ALUMINA INSERT.

Classifications

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

Product Code Device Name
MRA Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented