Clearance Summary
PHILIPS INTEGRIS 3D RA OPTION received FDA 510(k) clearance under submission number K983877, sponsored by Philips Medical Systems North America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1998-12-21.
- Submission: K983877
- Applicant / Sponsor: Philips Medical Systems North America, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1600
- Decision date: 1998-12-21
Classification & Regulation
This clearance is catalogued under FDA product code IZI and 21 CFR 892.1600, within the Radiology review panel as a Class II device.