Clearance Summary
DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3 received FDA 510(k) clearance under submission number K014001, sponsored by Oral Osteodistraction, L.P.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-02-04.
- Submission: K014001
- Applicant / Sponsor: Oral Osteodistraction, L.P.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4760
- Decision date: 2003-02-04
Classification & Regulation
This clearance is catalogued under FDA product code MQN and 21 CFR 872.4760, within the Dental review panel as a Class II device.