Clearance Summary
Patient Positioning System received FDA 510(k) clearance under submission number K170502, sponsored by Forte Automation Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-04-13.
- Submission: K170502
- Applicant / Sponsor: Forte Automation Systems, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5770
- Decision date: 2017-04-13
Classification & Regulation
This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.