K771418 is an FDA 510(k) clearance for the PIN RETRACTORS. This device is classified as a Pin, Fixation, Smooth (Class II - Special Controls, product code HTY).
Submitted by Stryker Corp. (Mchenry, US). The FDA issued a Cleared decision on September 22, 1977, 52 days after receiving the submission on August 1, 1977.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K771418 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 01, 1977 |
| Decision Date | September 22, 1977 |
| Days to Decision | 52 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | HTY — Pin, Fixation, Smooth |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |