Spectranetics Laser Sheath (GlideLight/SLS)
FDA premarket approval P960042/S072 · decided 2024-09-05
Approval details
- PMA number
- P960042
- Supplement
- S072
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Spectranetics Laser Sheath (GlideLight/SLS)
- Generic name
- DEVICE, REMOVAL, PACEMAKER ELECTRODE, PERCUTANEOUS
- Applicant
- Spectranetics (Philips)
- Date received
- 2024-08-05
- Decision date
- 2024-09-05
- Days to decision
- 31 days
- Decision code
- OK30
- Product code
- MFA
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Colorado Springs, CO
- Statement
- implementation of manufacturing software
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