Tachy DF4 header core
FDA premarket approval P010012/S553 · decided 2022-04-13
Approval details
- PMA number
- P010012
- Supplement
- S553
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Tachy DF4 header core
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- Boston Scientific Corp
- Date received
- 2022-04-04
- Decision date
- 2022-04-13
- Days to decision
- 9 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Modify the process for the seal plug cavity of the Tachy DF4 header core.
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