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 |