Clearance Summary
PROcedure Rehearsal Studio received FDA 510(k) clearance under submission number K153705, sponsored by 3Dsystems, Simbionix Products. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-09-02.
- Submission: K153705
- Applicant / Sponsor: 3Dsystems, Simbionix Products
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2016-09-02
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.