The following data is part of a premarket notification filed by Wittenstein Intens Gmbh with the FDA for Fitbone Taa.
Device ID | K163368 |
510k Number | K163368 |
Device Name: | FITBONE TAA |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | WITTENSTEIN Intens GmbH Walter-Wittensstein-StraBe 1 Igersheim, DE 97999 |
Contact | Hartmut Kampa |
Correspondent | Dudley Rajapaksa Berlin Heart Inc. 200 Valleywood Rd Suite B100 The Woodlands, TX 77338 0 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-11-30 |
Decision Date | 2017-01-26 |
Summary: | summary |