FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Prosthesis, Finger, Semi-Constrained, Metal/Polymer
PMA: P240020
·
Supplement: S002
·
Decision Sep 5, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
Basic Information
- Device Name
- Prosthesis, Finger, Semi-Constrained, Metal/Polymer
- Trade Name
- TOUCH® CMC 1 Prosthesis
- PMA Number
- P240020
- Supplement Number
- S002
- Device Class
- FDA Class 3
- Product Code
- SFA
- Generic Name
- Prosthesis, finger, semi-constrained, metal/polymer
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 5, 2025
- Date Received
- August 7, 2025
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
approval of the protocol for the post-approval study (PAS), TOUCH CMC 1 New Enrollment Study. The PAS protocol has been submitted to comply with the conditions of approval outlined in our approval order for P240020.
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 |
|---|---|---|---|
| SFA | Prosthesis, Finger, Semi-Constrained, Metal/Polymer | FDA class 3 | Unknown |