FDA 510(k) Applications Submitted by PAUL L SPEIDEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132740 | 09/03/2013 | SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM | SPINEFRONTIER, INC. |
| K133153 | 10/17/2013 | SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM | SPINEFRONTIER, INC. |
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