Last synced on 23 May 2025 at 11:06 pm

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
FDA Hosted 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
FDA Hosted 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