K031959 is an FDA 510(k) clearance for the STRYKER PLATING SYSTEM PERIARTICULAR PLATES. This device is classified as a Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite (Class II - Special Controls, product code LXT).
Submitted by Howmedica Osteonics Corp. (Allendale, US). The FDA issued a Cleared decision on July 25, 2003, 30 days after receiving the submission on June 25, 2003.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K031959 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 25, 2003 |
| Decision Date | July 25, 2003 |
| Days to Decision | 30 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | LXT — Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |