Clearance Summary
Waypoint GPS received FDA 510(k) clearance under submission number K222106, sponsored by Waypoint Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2023-05-12.
- Submission: K222106
- Applicant / Sponsor: Waypoint Orthopedics, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1820
- Decision date: 2023-05-12
Classification & Regulation
This clearance is catalogued under FDA product code QWP and 21 CFR 874.1820, within the Ear, Nose, Throat review panel as a Class II device.