Vertelink Corporation - FDA 510(k) Cleared Devices
Recent clearances: VERTELINK KOBRA SPINAL FIXATION SYSTEM, PATHWAY ACCESS SHEATH CATHETER, PATHWAY ACCESS SHEATH CATHETER
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vertelink Corporation Gastroenterology & Urology ✕
1 devices