TELIGEN
FDA premarket approval P960040/S209 · decided 2009-12-22
Approval details
- PMA number
- P960040
- Supplement
- S209
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- TELIGEN
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2009-11-25
- Decision date
- 2009-12-22
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- ADDITION OF TWO NEW ACCEPTANCE ACTIVITIES TO THE FINAL INSPECTION AT THE SUPPLIER.
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