Clearance Summary
SERIES II X3 LARGE DIAMETER ACCETABULAR INSERTS received FDA 510(k) clearance under submission number K103124, sponsored by Stryker Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-11-19.
- Submission: K103124
- Applicant / Sponsor: Stryker Corporation
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3358
- Decision date: 2010-11-19
Classification & Regulation
This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.