510(k) K162559
K162559 is an FDA 510(k) premarket notification submitted by Biomet, Inc. for the device "Move Forward 3D Motion Simulation Service". The FDA issued a decision of Substantially Equivalent on Mar 31, 2017. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Biomet, Inc. has 443 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 31, 2017
- Date Received
- Sep 14, 2016
- 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)