INTERTACH(R) FAMILY OF PULSE GENERATORS
FDA premarket approval P860007/S016 · decided 1996-05-21
Approval details
- PMA number
- P860007
- Supplement
- S016
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- INTERTACH(R) FAMILY OF PULSE GENERATORS
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
- Applicant
- Boston Scientific
- Date received
- 1995-09-18
- Decision date
- 1996-05-21
- Days to decision
- 246 days
- Decision code
- APPR
- Product code
- LWW
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- ALTERNATE STERILIZATION PROCESS
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