The following data is part of a premarket notification filed by Stryker Gmbh with the FDA for Variax 2 Compression Plating System.
Device ID | K170727 |
510k Number | K170727 |
Device Name: | VariAx 2 Compression Plating System |
Classification | Plate, Fixation, Bone |
Applicant | Stryker GmbH 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Tina Mornak |
Correspondent | Tina Mornak 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 | 2017-03-09 |
Decision Date | 2017-06-22 |
Summary: | summary |