The following data is part of a premarket notification filed by Stuckenbrock Medizintechnik Gmbh with the FDA for Ixos Radius Plate System.
Device ID | K171624 |
510k Number | K171624 |
Device Name: | IXOS Radius Plate System |
Classification | Plate, Fixation, Bone |
Applicant | Stuckenbrock Medizintechnik GmbH Lessingstraße 50 Tuttlingen, DE 78532 |
Contact | Fabian Stuckenbrock |
Correspondent | Fabian Stuckenbrock Stuckenbrock Medizintechnik GmbH Lessingstraße 50 Tuttlingen, DE 78532 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-02 |
Decision Date | 2018-03-29 |
Summary: | summary |