MODEL 1256D META MV CARDIAC PULSE GENERATOR
FDA premarket approval P900070/S019 · decided 1997-04-29
Approval details
- PMA number
- P900070
- Supplement
- S019
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MODEL 1256D META MV CARDIAC PULSE GENERATOR
- Generic name
- implantable pacemaker Pulse-generator
- Applicant
- St. Jude Medical, Cardiac Rhythm Management Divisi
- Date received
- 1997-04-14
- Decision date
- 1997-04-29
- Days to decision
- 15 days
- Decision code
- APPR
- Product code
- DXY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- APPROVAL FOR AN ALTERNATE MANUFACTURING SITE FOR MODEL 9602 PROGRAMMER. THE SITE IS LOCATED AT PACESETTER, INC., 15900 VALLEY VIEW CT., SYLMAR, CA
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