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Vertelink Corporation

FDA Regulatory Profile

Vertelink Corporation appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 12, 2003.

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

FDA data resources