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Spirus Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K080050SPIRUS MEDICAL ENDO-EASE ENDOSCOPIC OVERTUBEMay 6, 2008
K080042SPIRUS MEDICAL SURGICAL INSTRUMENTApril 3, 2008
K062805MODIFICATION TO ENDO-EASEOctober 13, 2006
K060235ENDO-EASE ENDOSCOPIC OVERTUBEAugust 4, 2006
K052084ENDO-EASE ENDOSCOPIC OVERTUBESeptember 14, 2005