Waypoint GPS— 510(k) K222106
Substantially EquivalentWaypoint Orthopedics, Inc.
FDA 510(k) clearance K222106 for Waypoint GPS, Substantially Equivalent on 2023-05-12. Applicant: Waypoint Orthopedics, Inc.. Device class: 2.
Clearance details
- Applicant
- Waypoint Orthopedics, Inc.
- Product code
- Code QWP
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Malvern, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.