Clearance Summary
VariTrax Sternal CircumFixation System received FDA 510(k) clearance under submission number K232986, sponsored by Circumfix Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-01-30.
- Submission: K232986
- Applicant / Sponsor: Circumfix Solutions, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3010
- Decision date: 2024-01-30
Classification & Regulation
This clearance is catalogued under FDA product code JDQ and 21 CFR 888.3010, within the Orthopedic review panel as a Class II device.