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MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES

Page Type
Cleared 510(K)
510(k) Number
K010511
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2001
Days to Decision
8 days
Submission Type
Summary

MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES

Page Type
Cleared 510(K)
510(k) Number
K010511
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2001
Days to Decision
8 days
Submission Type
Summary