DIAMONDBACK 360® and Diamondback 360 Precision Coronary Orbital Atherectomy System (OAS)
FDA premarket approval P130005/S045 · decided 2025-04-24
Approval details
- PMA number
- P130005
- Supplement
- S045
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- DIAMONDBACK 360® and Diamondback 360 Precision Coronary Orbital Atherectomy System (OAS)
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Applicant
- Cardiovascular Systems, Inc.
- Date received
- 2025-03-27
- Decision date
- 2025-04-24
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MCX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Change to include alternate Tyvek pouch coating material suppliers
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