ELLIPSE
FDA premarket approval P910023/S377 · decided 2016-12-19
Approval details
- PMA number
- P910023
- Supplement
- S377
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ELLIPSE
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- ABBOTT MEDICAL
- Date received
- 2016-11-30
- Decision date
- 2016-12-19
- Days to decision
- 19 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- Implementation of an automated epoxy dispensing system for use during pulse generator assembly.
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|---|---|---|
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