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ANGIOJET ULTRA; XMI (105041), XVG (105042) AND SPIROFLEX (106553) THROMBECTOMY SETS

Page Type
Cleared 510(K)
510(k) Number
K072769
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2007
Days to Decision
47 days
Submission Type
Summary

ANGIOJET ULTRA; XMI (105041), XVG (105042) AND SPIROFLEX (106553) THROMBECTOMY SETS

Page Type
Cleared 510(K)
510(k) Number
K072769
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2007
Days to Decision
47 days
Submission Type
Summary