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 |