510(k) K141787
K141787 is an FDA 510(k) premarket notification submitted by Orfit Industries NV for the device "SAGITTILT". The FDA issued a decision of Substantially Equivalent on August 7, 2014. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Orfit Industries NV has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 2014
- Date Received
- July 2, 2014
- 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