510(k) K203696
K203696 is an FDA 510(k) premarket notification submitted by Radiobotics Aps for the device "RBknee". The FDA issued a decision of Substantially Equivalent on Aug 27, 2021. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 27, 2021
- Date Received
- Dec 18, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)