FDA 510(k) K132578, INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM, by Boston Scientific Corp
FDA 510(k) K132578, INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM, by Boston Scientific Corp
Device Classification Name: Device, Vascular, For Promoting Embolization
510(k) Number: K132578
Device Name: INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM
Applicant: Boston Scientific Corp
Regulation Number: 870.3300
Classification Product Code: KRD
Date Received: 08/16/2013
Decision Date: 09/13/2013
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
510k Review Panel: Cardiovascular
Total number of pages: 154
Fully redacted pages: 20
Content pages: 134
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