The following data is part of a premarket notification filed by Medos International Sarl with the FDA for Distal Volar Radius Plating Systems.
Device ID | K112345 |
510k Number | K112345 |
Device Name: | DISTAL VOLAR RADIUS PLATING SYSTEMS |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite |
Applicant | MEDOS INTERNATIONAL SARL 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 |
Contact | Suzana Otano |
Correspondent | Suzana Otano MEDOS INTERNATIONAL SARL 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 |
Product Code | LXT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-15 |
Decision Date | 2011-10-31 |