ANTHEM/FRONTIER II CRT-PS
FDA premarket approval P030035/S055 · decided 2009-06-12
Approval details
- PMA number
- P030035
- Supplement
- S055
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ANTHEM/FRONTIER II CRT-PS
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Applicant
- ABBOTT MEDICAL
- Date received
- 2009-05-14
- Decision date
- 2009-06-12
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- NKE
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- ALTERNATE SUPPLIER FOR THE LOW VOLTAGE HYBRID ASSEMBLY.
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