K810045 is an FDA 510(k) clearance for the I.M. RETROGRADE BLADES. This device is classified as a Blade, Saw, General & Plastic Surgery, Surgical (Class I - General Controls, product code GFA).
Submitted by Hogan & Hartson (Mchenry, US). The FDA issued a Cleared decision on February 12, 1981, 35 days after receiving the submission on January 8, 1981.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4820.
| 510(k) Number | K810045 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 08, 1981 |
| Decision Date | February 12, 1981 |
| Days to Decision | 35 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | GFA — Blade, Saw, General & Plastic Surgery, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4820 |