ELA IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
FDA premarket approval P060027/S016 · decided 2009-12-14
Approval details
- PMA number
- P060027
- Supplement
- S016
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ELA IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2009-11-16
- Decision date
- 2009-12-14
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- CHANGE IN THE LOCATION FOR MANUFACTURING THE HYBRID ELECTRONIC MODULE COMPONENT.
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.