FDA 510(k) Applications Submitted by PAMELA SNYDER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990959 | 03/22/1999 | K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM | SPINEOLOGY, INC. |
| K002371 | 07/27/2000 | K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM | SPINEOLOGY, INC. |
| K033953 | 12/22/2003 | OPTIMESH 500E CEMENT RESTRICTOR | SPINEOLOGY, INC. |
| K014200 | 12/21/2001 | OPTIMESH | SPINEOLOGY, INC. |
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