SLS II/GLIDELIGHT CATHETERS
FDA premarket approval P960042/S055 · decided 2017-01-05
Approval details
- PMA number
- P960042
- Supplement
- S055
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- SLS II/GLIDELIGHT CATHETERS
- Generic name
- DEVICE, REMOVAL, PACEMAKER ELECTRODE, PERCUTANEOUS
- Applicant
- Spectranetics (Philips)
- Date received
- 2016-12-08
- Decision date
- 2017-01-05
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MFA
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Colorado Springs, CO
- Statement
- Use of a replacement laser micrometer inspection tool.
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