VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR
FDA premarket approval P910077/S184 · decided 2021-05-10
Approval details
- PMA number
- P910077
- Supplement
- S184
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2021-04-30
- Decision date
- 2021-05-10
- Days to decision
- 10 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Add a new pallet sterilization chamber at the Arden Hills facility to increase sterilization capacity.
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