PMA P900056S216
- Device
- Rotablator and ROTAPRO Rotational Atherectomy System
- Applicant
- Boston Scientific Corp
- PMA number
- P900056
- Supplement
- S216
- Product code
- MCX
- Decision date
- 2024-03-15
- Classification
- Cardiovascular
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Approval order statement
- approval to add an alternate supplier for the ROTAPRO Advancers’ Dowel Pin component
Current openFDA PMA Record#
- Device
- Rotablator and ROTAPRO Rotational Atherectomy System
- Applicant
- Boston Scientific Corp
- PMA number
- P900056
- Supplement
- S216
- Product code
- MCX
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Decision date
- 2024-03-15
- Decision code
- OK30
- Date received
- 2024-02-16
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- approval to add an alternate supplier for the ROTAPRO Advancers’ Dowel Pin component