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ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180416
510(k) Type
Traditional
Applicant
Cardiovascular Systems Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
61 days
Submission Type
Summary

ViperWire Advance Guide Wire, Stealth 360 Orbital Peripheral Atherectomy Device (PAD), DIAMONDBACK 360 Peripheral Atherectomy System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180416
510(k) Type
Traditional
Applicant
Cardiovascular Systems Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2018
Days to Decision
61 days
Submission Type
Summary