Clearance Summary
VERTAPLEX HV (SINGLE PACK AND DUAL PACK) received FDA 510(k) clearance under submission number K091606, sponsored by Stryker Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-10-23.
- Submission: K091606
- Applicant / Sponsor: Stryker Corp.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3027
- Decision date: 2009-10-23
Classification & Regulation
This clearance is catalogued under FDA product code NDN and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.