KFK — Saw, Pneumatically Powered Class I
FDA product code KFK covers "Saw, Pneumatically Powered", a Class I medical device regulated under 21 CFR 878.4820. Submissions are reviewed by the General, Plastic Surgery panel. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KFK
- Device Class
- Class I
- Regulation Number
- 878.4820
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K893949 | medmark | #157 EXAM LIGHT | August 7, 1989 |
| K894301 | micro surgical instruments | MICRO-AIRE STERNUM SAW 4800 | August 3, 1989 |
| K870157 | micro-aire surgical instruments | OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER | February 24, 1987 |
| K801737 | amsco | STERNUM SAW | August 20, 1980 |