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SPIDERX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K052659
510(k) Type
Traditional
Applicant
EV3 INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2006
Days to Decision
143 days
Submission Type
Summary

SPIDERX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K052659
510(k) Type
Traditional
Applicant
EV3 INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2006
Days to Decision
143 days
Submission Type
Summary