Clearance Summary
STRYKER (R) PATIENT SPECIFIC POLYMER IMPLANT received FDA 510(k) clearance under submission number K111065, sponsored by Howmedica Osteonics Corp. Dba Stryker Orthopeadics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-07-14.
- Submission: K111065
- Applicant / Sponsor: Howmedica Osteonics Corp. Dba Stryker Orthopeadics
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5320
- Decision date: 2011-07-14
Classification & Regulation
This clearance is catalogued under FDA product code GWO and 21 CFR 882.5320, within the Neurology review panel as a Class II device.