Last synced on 14 November 2025 at 11:06 pm

Rotarex Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K211738
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2021
Days to Decision
99 days
Submission Type
Summary

Rotarex Atherectomy System

Page Type
Cleared 510(K)
510(k) Number
K211738
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2021
Days to Decision
99 days
Submission Type
Summary