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 |