Clearance Summary
OMNIAXIAL CONNECTOR received FDA 510(k) clearance under submission number K993926, sponsored by Ortho Tec, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-12-17.
- Submission: K993926
- Applicant / Sponsor: Ortho Tec, LLC
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 1999-12-17
Classification & Regulation
This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.