Clearance Summary
DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM received FDA 510(k) clearance under submission number K061166, sponsored by Biowave Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2006-08-15.
- Submission: K061166
- Applicant / Sponsor: Biowave Corporation
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 2006-08-15
Classification & Regulation
This clearance is catalogued under FDA product code NHI and 21 CFR 882.5890, within the Neurology review panel as a Class II device.