Last synced on 25 January 2026 at 3:41 am

DIAMONDBACK 360 Peripheral Orbital Atherectomy System, DIAMONDBACK 360 Peripheral Orbital Atherectomy System, Exchangeable Series, Stealth 360 Peripheral Orbital Atherectomy System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220109
510(k) Type
Special
Applicant
Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2022
Days to Decision
47 days
Submission Type
Summary

DIAMONDBACK 360 Peripheral Orbital Atherectomy System, DIAMONDBACK 360 Peripheral Orbital Atherectomy System, Exchangeable Series, Stealth 360 Peripheral Orbital Atherectomy System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220109
510(k) Type
Special
Applicant
Cardiovascular Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2022
Days to Decision
47 days
Submission Type
Summary