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 |