Last synced on 14 November 2025 at 11:06 pm

TRANSFORM OCCLUSION BALLOON CATHETER (COMPLIANT AND SUPER COMPLIANT

Page Type
Cleared 510(K)
510(k) Number
K122576
510(k) Type
Traditional
Applicant
STRYKER NEUROVASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2013
Days to Decision
141 days
Submission Type
Summary

TRANSFORM OCCLUSION BALLOON CATHETER (COMPLIANT AND SUPER COMPLIANT

Page Type
Cleared 510(K)
510(k) Number
K122576
510(k) Type
Traditional
Applicant
STRYKER NEUROVASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2013
Days to Decision
141 days
Submission Type
Summary