FDA 510(k) Applications Submitted by ORTHOTEC,LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011807 | 06/11/2001 | SCS CLARIS SPINAL SCREWS, TYPES V,G,E | ORTHOTEC,LLC |
| K021919 | 06/11/2002 | SCS CLARIS SPINAL SYSTEM,REXTENDED OMNIAXIAL CONNECTOR-,MEDIUM, MODEL CO05, SCS CLARIS SPINAL SYSTEM,EXTENDED OMNIAXIALO | ORTHOTEC,LLC |
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