FDA 510(k) Applications Submitted by JOSH KAUFMANN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100757 | 03/17/2010 | TILOCK PEDICLE SCREW SYSTEM | GENESYS SPINE |
| K103034 | 10/13/2010 | GENESYS SPINE INTERBODY FUSION SYSTEM | GENESYS SPINE |
| K092531 | 08/18/2009 | SPINE360 ANTERIOR CERVICAL PLATE SYSTEM | SPINE 360 |
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