Clearance Summary
Oxiplex® received FDA 510(k) clearance under submission number DEN240038, sponsored by Fziomed, Inc.. The device was reviewed via the Direct premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-06-17.
- Submission: DEN240038
- Applicant / Sponsor: Fziomed, Inc.
- Clearance pathway: Direct
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3047
- Decision date: 2025-06-17
Classification & Regulation
This clearance is catalogued under FDA product code QVL and 21 CFR 888.3047, within the Orthopedic review panel as a Class II device.