Diamondback 360 Coronary Orbital Atherectomy System
FDA premarket approval P130005/S035 · decided 2022-03-11
Approval details
- PMA number
- P130005
- Supplement
- S035
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Diamondback 360 Coronary Orbital Atherectomy System
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Applicant
- Cardiovascular Systems, Inc.
- Date received
- 2022-02-18
- Decision date
- 2022-03-11
- Days to decision
- 21 days
- Decision code
- OK30
- Product code
- MCX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Introducing alternate suppliers for different non-patient-contacting device components.
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