K934390 is an FDA 510(k) clearance for the OSCILLATING BONE SAW BLADE, 6200 SERIES. This device is classified as a Blade, Saw, General & Plastic Surgery, Surgical (Class I - General Controls, product code GFA).
Submitted by Boehringer Laboratories (Norristown, US). The FDA issued a Cleared decision on January 26, 1994, 139 days after receiving the submission on September 9, 1993.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4820.
| 510(k) Number | K934390 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 09, 1993 |
| Decision Date | January 26, 1994 |
| Days to Decision | 139 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GFA — Blade, Saw, General & Plastic Surgery, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4820 |