FDA 510(k) Applications Submitted by TRINITY ORTHOPEDICS, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070295 | 01/31/2007 | SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM | TRINITY ORTHOPEDICS, LLC |
| K081790 | 06/25/2008 | MODIFICATION TO SINGLE PLANAR MULTI AXIS (SPMA) PEDICLE SCREW SYSTEM | TRINITY ORTHOPEDICS, LLC |
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