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PIONEER PLUS CATHETER, MODEL PLUS 120

Page Type
Cleared 510(K)
510(k) Number
K101777
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2010
Days to Decision
28 days
Submission Type
Summary

PIONEER PLUS CATHETER, MODEL PLUS 120

Page Type
Cleared 510(K)
510(k) Number
K101777
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2010
Days to Decision
28 days
Submission Type
Summary