510(k) K181112
K181112 is an FDA 510(k) premarket notification submitted by Orchestrate 3D for the device "Orchestrate 3D". The FDA issued a decision of Substantially Equivalent on Nov 26, 2018. The device falls under product code PNN (Orthodontic Software), a Class II device regulated under 21 CFR 872.5470.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 26, 2018
- Date Received
- Apr 27, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Orthodontic Software
- Device Class
- Class II
- Regulation Number
- 872.5470
- Review Panel
- DE
- Submission Type
- 510(k)
The device is software that is to be used for the diagnosis and treatment planning of orthodontic patients and conditions. It may include orthodontic output devices used for the treatment of orthodontics. The device is intended for prescription use only.