INTERTACH(R)II MODELS 262-16
FDA premarket approval P860007/S012 · decided 1993-08-04
Approval details
- PMA number
- P860007
- Supplement
- S012
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- INTERTACH(R)II MODELS 262-16
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
- Applicant
- Boston Scientific
- Date received
- 1993-05-03
- Decision date
- 1993-08-04
- Days to decision
- 93 days
- Decision code
- APPR
- Product code
- LWW
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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