EMBLEM Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) Anneal Parameters
FDA premarket approval P110042/S182 · decided 2023-05-12
Approval details
- PMA number
- P110042
- Supplement
- S182
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- EMBLEM Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) Anneal Parameters
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific Corporation
- Date received
- 2023-04-14
- Decision date
- 2023-05-12
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Change the annealing process of the EMBLEM S-ICD pulse generator case halves to align with industry standards.
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