K850483 is an FDA 510(k) clearance for the MICRO-AIRE STERNUM SAW REPLACEMENT BLADES. This device is classified as a Blade, Saw, Surgical, Cardiovascular (Class I - General Controls, product code DWH).
Submitted by Micro-Aire Surgical Instruments, Inc. (San Fernando, US). The FDA issued a Cleared decision on March 1, 1985, 22 days after receiving the submission on February 7, 1985.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4820.
| 510(k) Number | K850483 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 07, 1985 |
| Decision Date | March 01, 1985 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | DWH — Blade, Saw, Surgical, Cardiovascular |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4820 |