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 | Device Class | Medical Specialty |
|---|---|---|---|
| PNW | Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant | FDA class 3 | Unknown |