FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Prosthesis, Ankle, Uncemented, Non-Constrained
PMA: P160036
·
Supplement: S001
·
Decision Nov 29, 2019
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Prosthesis, Ankle, Uncemented, Non-Constrained
- Trade Name
- Hintermann Series H3 Total Ankle Replacement System
- PMA Number
- P160036
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- NTG
- Generic Name
- Prosthesis, ankle, uncemented, non-constrained
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- November 29, 2019
- Date Received
- July 1, 2019
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval for the post-approval study protocols for the two post-approval studies.
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 |
|---|---|---|---|
| NTG | Prosthesis, Ankle, Uncemented, Non-Constrained | FDA class 3 | Unknown |