INGEVITY Distal Tip Laser Weld Process
FDA premarket approval P150012/S072 · decided 2019-03-14
Approval details
- PMA number
- P150012
- Supplement
- S072
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- INGEVITY Distal Tip Laser Weld Process
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2019-02-15
- Decision date
- 2019-03-14
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Modifications of the distal tip laser weld, laser weld fixtures, processes, and software used for the helix to coupler weld.
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