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

Page Type
Cleared 510(K)
PDF
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
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