CORVUS

System, Planning, Radiation Therapy Treatment

Best Nomos

The following data is part of a premarket notification filed by Best Nomos with the FDA for Corvus.

Pre-market Notification Details

• Device ID: K201350
• 510k Number: K201350
• Device Name: CORVUS
• Classification: System, Planning, Radiation Therapy Treatment
• Applicant: Best Nomos One Best Drive Pittsburgh, PA 15202
• Contact: Vineet Gupta
• Correspondent: Vineet Gupta; Best Nomos One Best Drive Pittsburgh, PA 15202
• Product Code: MUJ
• CFR Regulation Number: 892.5050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2020-05-21
• Decision Date: 2020-09-20