FDA 510(k) Applications Submitted by T. A. COX
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001476 | 05/11/2000 | TORQUE INSTRUMENT, MODEL 8500 | SPINALIGHT, INC. |
| K955540 | 12/05/1995 | HAND HELD ATLAS INSTRUMENT | SPINALIGHT, INC. |
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