Clearance Summary
AVS ARIA NEUROMONITORING PROBE AND AVS ARIA PROBE DILATORS received FDA 510(k) clearance under submission number K110419, sponsored by Stryker Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-07-28.
- Submission: K110419
- Applicant / Sponsor: Stryker Spine
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.1350
- Decision date: 2011-07-28
Classification & Regulation
This clearance is catalogued under FDA product code GXZ and 21 CFR 882.1350, within the Neurology review panel as a Class II device.