KDA — Prosthesis, Ptfe/Carbon-Fiber Class II
FDA product code KDA covers "Prosthesis, Ptfe/Carbon-Fiber", a Class II medical device regulated under 21 CFR 878.3500. Submissions are reviewed by the General, Plastic Surgery panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KDA
- Device Class
- Class II
- Regulation Number
- 878.3500
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K861806 | medcomp technologies | MEDCARE SUTURE SCISSORS (SUTURE/GAUZE WEIGHT) | May 23, 1986 |