Clearance Summary
BIOBALL DELTA CERAMIC HEADS, MULTICUP PE INLAY STANDARD received FDA 510(k) clearance under submission number K141377, sponsored by Merete Medical GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-11-21.
- Submission: K141377
- Applicant / Sponsor: Merete Medical GmbH
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3353
- Decision date: 2014-11-21
Classification & Regulation
This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.