510(k) K140337
K140337 is an FDA 510(k) premarket notification submitted by Synaptive Medical, Inc. for the device "BRIGHTMATTER PLANNING SOFTWARE". The FDA issued a decision of Substantially Equivalent on June 2, 2014. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Synaptive Medical, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 2014
- Date Received
- February 10, 2014
- 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