The following data is part of a premarket notification filed by Orthohelix Surgical Designs, Inc. with the FDA for Css Cannulated Screw System.
| Device ID | K060428 |
| 510k Number | K060428 |
| Device Name: | CSS CANNULATED SCREW SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET Akron, OH 44313 |
| Contact | Lee A Strnad |
| Correspondent | Lee A Strnad ORTHOHELIX SURGICAL DESIGNS, INC. 1815 W. MARKET Akron, OH 44313 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-02-21 |
| Decision Date | 2006-03-07 |
| Summary: | summary |