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Vertelink Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K032102VERTELINK KOBRA SPINAL FIXATION SYSTEMDecember 12, 2003
K030734PATHWAY ACCESS SHEATH CATHETERSeptember 10, 2003
K030662PATHWAY ACCESS SHEATH CATHETERSeptember 3, 2003