The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for Stryker Plating System Periarticular Plates.
| Device ID | K031959 |
| 510k Number | K031959 |
| Device Name: | STRYKER PLATING SYSTEM PERIARTICULAR PLATES |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
| Applicant | HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Contact | Vivian Kelly |
| Correspondent | Vivian Kelly HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Product Code | LXT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-06-25 |
| Decision Date | 2003-07-25 |
| Summary: | summary |