SPIDERFX EMBOLIC PROTECTION DEVICE— 510(k) K063785

Substantially Equivalent

Ev3, Inc.

FDA 510(k) clearance K063785 for SPIDERFX EMBOLIC PROTECTION DEVICE, Substantially Equivalent on 2007-01-19. Applicant: Ev3, Inc..

Clearance details

Applicant: Ev3, Inc.
Product code: Code NFA
Advisory panel: Cardiovascular
Date received: 2006-12-21
Decision date: 2007-01-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Plymouth, MN, US

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