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TurboHawk Plus Directional Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K212027
510(k) Type
Traditional
Applicant
Medtronic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2021
Days to Decision
56 days
Submission Type
Summary

TurboHawk Plus Directional Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K212027
510(k) Type
Traditional
Applicant
Medtronic, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2021
Days to Decision
56 days
Submission Type
Summary