Clearance Summary
STRYKER ORTHOPOWER 90 & ORTHOPOWER 90 SYSTEM II received FDA 510(k) clearance under submission number K863447, sponsored by Stryker Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1986-09-29.
- Submission: K863447
- Applicant / Sponsor: Stryker Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1986-09-29
Classification & Regulation
This clearance is catalogued under FDA product code GET and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.