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 |