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 |