K872490 is an FDA 510(k) clearance for the 1.1 SCREWDRIVERS. This device is classified as a Screwdriver, Surgical (Class I - General Controls, product code LRZ).
Submitted by Micro-Aire Surgical Instruments, Inc. (San Fernando, US). The FDA issued a Cleared decision on July 23, 1987, 30 days after receiving the submission on June 23, 1987.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4800.
| 510(k) Number | K872490 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 23, 1987 |
| Decision Date | July 23, 1987 |
| Days to Decision | 30 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | LRZ — Screwdriver, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4800 |