Clearance Summary
JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT received FDA 510(k) clearance under submission number K060815, sponsored by Bioform Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2006-04-18.
- Submission: K060815
- Applicant / Sponsor: Bioform Medical, Inc.
- Clearance pathway: Special
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3620
- Decision date: 2006-04-18
Classification & Regulation
This clearance is catalogued under FDA product code MIX and 21 CFR 874.3620, within the Ear, Nose, Throat review panel as a Class II device.