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SPIDERFX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K063785
510(k) Type
Special
Applicant
EV3 INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2007
Days to Decision
29 days
Submission Type
Summary

SPIDERFX EMBOLIC PROTECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K063785
510(k) Type
Special
Applicant
EV3 INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2007
Days to Decision
29 days
Submission Type
Summary