Clearance Summary
STRYKER VENOM ELECTRODES AND CANNULAE received FDA 510(k) clearance under submission number K123178, sponsored by Stryker Instruments, Instruments Div.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2013-03-28.
- Submission: K123178
- Applicant / Sponsor: Stryker Instruments, Instruments Div.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4725
- Decision date: 2013-03-28
Classification & Regulation
This clearance is catalogued under FDA product code GXI and 21 CFR 882.4725, within the Neurology review panel as a Class II device.