PMA P900056S070
- Device
- ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM
- Applicant
- Boston Scientific Corp
- PMA number
- P900056
- Supplement
- S070
- Product code
- MCX
- Decision date
- 2002-04-11
- Classification
- Catheter, Coronary, Atherectomy
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Approval order statement
- CHANGE IN THE MANUFACTURING PROCESS TO ELIMINATE THE POST-STERILIZATION VERIFICATION PROCESS.
Current openFDA PMA Record#
- Device
- ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM
- Applicant
- Boston Scientific Corp
- PMA number
- P900056
- Supplement
- S070
- Product code
- MCX
- Generic name
- CATHETER, CORONARY, ATHERECTOMY
- Decision date
- 2002-04-11
- Decision code
- OK30
- Date received
- 2002-03-12
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE IN THE MANUFACTURING PROCESS TO ELIMINATE THE POST-STERILIZATION VERIFICATION PROCESS.