INTERTACH(R)II MODELS 262-16/262-16R DISCON.TEST
FDA premarket approval P860007/S010 · decided 1993-01-11
Approval details
- PMA number
- P860007
- Supplement
- S010
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- INTERTACH(R)II MODELS 262-16/262-16R DISCON.TEST
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
- Applicant
- Boston Scientific
- Date received
- 1992-07-10
- Decision date
- 1993-01-11
- Days to decision
- 185 days
- Decision code
- APPR
- Product code
- LWW
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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