Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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