Clearance Summary
BIOMET ACCESS SYSTEM received FDA 510(k) clearance under submission number K132373, sponsored by Biomet Spine (Aka Ebi, LLC). The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2014-03-27.
- Submission: K132373
- Applicant / Sponsor: Biomet Spine (Aka Ebi, LLC)
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1820
- Decision date: 2014-03-27
Classification & Regulation
This clearance is catalogued under FDA product code PDQ and 21 CFR 874.1820, within the Ear, Nose, Throat review panel as a Class II device.