The following data is part of a premarket notification filed by Stryker Gmbh with the FDA for Axsos 3 Ti; Stryker Plating System.
| Device ID | K162439 |
| 510k Number | K162439 |
| Device Name: | AxSOS 3 Ti; Stryker Plating System |
| Classification | Plate, Fixation, Bone |
| Applicant | STRYKER GMBH 325 CORPORATE DRIVE Mahwah, NJ 07430 |
| Contact | Irene Bacalocostantis |
| Correspondent | Irene Bacalocostantis STRYKER GMBH 325 CORPORATE DRIVE Mahwah, NJ 07430 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-08-31 |
| Decision Date | 2017-02-03 |
| Summary: | summary |