The following data is part of a premarket notification filed by Merete Gmbh with the FDA for Osteobridge™ Idsf System.
| Device ID | K181026 |
| 510k Number | K181026 |
| Device Name: | OsteoBridge™ IDSF System |
| Classification | Rod, Fixation, Intramedullary And Accessories |
| Applicant | Merete GmbH Alt-Lankwitz 102 Berlin, DE 12247 |
| Contact | Paul Munch |
| Correspondent | Paul Munch Merete GmbH Alt-Lankwitz 102 Berlin, DE 12247 |
| Product Code | HSB |
| CFR Regulation Number | 888.3020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-04-18 |
| Decision Date | 2018-10-17 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OSTEOBRIDGE 86180106 4636001 Live/Registered |
ARISTOTECH INDUSTRIES GMBH 2014-01-30 |
![]() OSTEOBRIDGE 77009670 3354525 Dead/Cancelled |
ARISTOTECH INDUSTRIES GMBH 2006-09-28 |