Clearance Summary
LG HEX PROSTHETICS received FDA 510(k) clearance under submission number K954539, sponsored by The Implant Center of the Palm Beaches. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-10-30.
- Submission: K954539
- Applicant / Sponsor: The Implant Center of the Palm Beaches
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 1995-10-30
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.