FDA 510(k) Applications Submitted by VERTELINK CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030662 | 03/03/2003 | PATHWAY ACCESS SHEATH CATHETER | VERTELINK CORPORATION |
| K030734 | 03/10/2003 | PATHWAY ACCESS SHEATH CATHETER | VERTELINK CORPORATION |
| K032102 | 07/08/2003 | VERTELINK KOBRA SPINAL FIXATION SYSTEM | VERTELINK CORPORATION |
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