Last synced on 11 July 2025 at 11:06 pm

ViperWire Advance Guide Wire, Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Orbital PAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151260
510(k) Type
Special
Applicant
Cardiovascular System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2015
Days to Decision
29 days
Submission Type
Summary

ViperWire Advance Guide Wire, Diamondback 360 Peripheral Orbital Atherectomy System, Stealth 360 Orbital PAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151260
510(k) Type
Special
Applicant
Cardiovascular System, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2015
Days to Decision
29 days
Submission Type
Summary