DIAMONDBACK 360 CORONARY ORIBITAL ATHERECTOMY SYSTEM (OAS)
FDA premarket approval P130005/S008 · decided 2015-06-25
Approval details
- PMA number
- P130005
- Supplement
- S008
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- DIAMONDBACK 360 CORONARY ORIBITAL ATHERECTOMY SYSTEM (OAS)
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Applicant
- Cardiovascular Systems, Inc.
- Date received
- 2015-04-10
- Decision date
- 2015-06-25
- Days to decision
- 76 days
- Decision code
- APPR
- Product code
- MCX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL TO CHANGE THE BLACK COLORANT USED IN THE ON/OFF BUTTON OF THE DIAMONDBACK 360 CORONARY ORBITAL ATHERECTOMY DEVICE.
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