The following data is part of a premarket notification filed by Stryker Gmbh with the FDA for Variax 2 System.
Device ID | K180500 |
510k Number | K180500 |
Device Name: | VariAx 2 System |
Classification | Screw, Fixation, Bone |
Applicant | Stryker GmbH 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Paul Nelson |
Correspondent | Paul Nelson Stryker GmbH 325 Corporate Drive Mahwah, NJ 07430 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-02-26 |
Decision Date | 2018-06-04 |
Summary: | summary |