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ROTAPRO Rotational Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K220962
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2022
Days to Decision
158 days
Submission Type
Summary

ROTAPRO Rotational Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K220962
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2022
Days to Decision
158 days
Submission Type
Summary