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Vesitec Medical, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K932925BONE ANCHOR FOR SOFT TISSUE ATTACHMENTApril 26, 1994
K931182VESITEC DRILL GUIDEJune 9, 1993
K931181VESITEC SUTURE PASSERMay 12, 1993