The following data is part of a premarket notification filed by Orthohelix Surgical Designs, Inc. with the FDA for Modular Foot System.
Device ID | K073624 |
510k Number | K073624 |
Device Name: | MODULAR FOOT SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET ST. SUITE 205 Akron, OH 44313 |
Contact | Derek Lewis |
Correspondent | Derek Lewis ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET ST. SUITE 205 Akron, OH 44313 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-12-26 |
Decision Date | 2008-03-20 |
Summary: | summary |