Last synced on 25 January 2026 at 3:41 am

TurboHawk Plus Directional Atherectomy System

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