FDA PMA FDA Class 3 Approved 🇺🇸 United States

Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

PMA: P150017 · Supplement: S003 · Decision Nov 1, 2016
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant
Trade Name
CARTIVA SYNTHETIC CARTILAGE IMPLANT
PMA Number
P150017
Supplement Number
S003
Device Class
FDA Class 3
Product Code
PNW
Generic Name
Prosthesis, metatarsophalangeal joint cartilage replacement implant
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
November 1, 2016
Date Received
August 15, 2016
Supplement Type
Real-Time Process
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for the addition of 8 and 20-unit shipping configurations to accommodate smaller orders.

Classifications

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

Product Code Device Name
PNW Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant