510(k) K171133
K171133 is an FDA 510(k) premarket notification submitted by Qfix for the device "Qfix® Abdominal/Thoracic Motion Control System,Qfix® SBRT Solution and Accessories". The FDA issued a decision of Substantially Equivalent on Jul 11, 2017. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Qfix has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 11, 2017
- Date Received
- Apr 17, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accelerator, Linear, Medical
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type
- 510(k)