The following data is part of a premarket notification filed by Orthohelix Surgical Designs, Inc. with the FDA for Mini Maxlock Extreme Plating System.
Device ID | K101962 |
510k Number | K101962 |
Device Name: | MINI MAXLOCK EXTREME PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ORTHOHELIX SURGICAL DESIGNS, INC. 1065 MEDINA ROAD SUITE 500 Medina, OH 44256 |
Contact | Derek Lewis |
Correspondent | Derek Lewis ORTHOHELIX SURGICAL DESIGNS, INC. 1065 MEDINA ROAD SUITE 500 Medina, OH 44256 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-07-13 |
Decision Date | 2010-09-27 |
Summary: | summary |