Clearance Summary
KNEEHAB XP CONTROLLER, MODEL 411 received FDA 510(k) clearance under submission number K092791, sponsored by Bio-Medical Research, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2009-12-30.
- Submission: K092791
- Applicant / Sponsor: Bio-Medical Research, Ltd.
- Clearance pathway: Special
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5850
- Decision date: 2009-12-30
Classification & Regulation
This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.