Prosthesis, Ptfe/Carbon-Fiber
FDA product code KDA · Class II (moderate risk) · 21 CFR 878.3500 · General, Plastic Surgery
1510(k) clearances
0PMA approvals
0recalls
Implantimplanted device
Manufacturers
510(k) clearances
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K861806 | Medcare Suture Scissors (Suture/Gauze Weight)KDA · Traditional | Medcomp Technologies, Inc. | 05/23/1986SE |