LRZ — Screwdriver, Surgical Class I
FDA Device Classification
Classification Details
- Product Code
- LRZ
- Device Class
- Class I
- Regulation Number
- 878.4800
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K896589 | optik | MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP | December 27, 1989 |
| K872490 | micro-aire surgical instruments | 1.1 SCREWDRIVERS | July 23, 1987 |
| K872387 | med-tool | STANDARD SCREW DRIVER | July 16, 1987 |