The following data is part of a premarket notification filed by Stryker with the FDA for Stryker Upper-face Axs Screws And Mid-face Axs Screws.
Device ID | K172572 |
510k Number | K172572 |
Device Name: | Stryker Upper-Face AXS Screws And Mid-Face AXS Screws |
Classification | Plate, Bone |
Applicant | Stryker 750 Trade Centre Way - Suite 200 Portage, MI 49002 |
Contact | Jonathan Schell |
Correspondent | Jonathan Schell Stryker 750 Trade Centre Way - Suite 200 Portage, MI 49002 |
Product Code | JEY |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-28 |
Decision Date | 2017-10-31 |
Summary: | summary |