Last synced on 23 May 2025 at 11:06 pm

Rotarex Atherectomy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242757
510(k) Type
Special
Applicant
Bard Peripheral Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2025
Days to Decision
140 days
Submission Type
Summary

Rotarex Atherectomy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242757
510(k) Type
Special
Applicant
Bard Peripheral Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2025
Days to Decision
140 days
Submission Type
Summary