K122313 is an FDA 510(k) clearance for the STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM. This device is classified as a Plate, Bone (Class II - Special Controls, product code JEY).
Submitted by Stryker (Portage, US). The FDA issued a Cleared decision on October 31, 2012, 91 days after receiving the submission on August 1, 2012.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4760.
| 510(k) Number | K122313 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 01, 2012 |
| Decision Date | October 31, 2012 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | JEY — Plate, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.4760 |