510(k) K170460
K170460 is an FDA 510(k) premarket notification submitted by Sorin Group Deutschland GmbH for the device "Sorin Connect". The FDA issued a decision of Substantially Equivalent on June 8, 2017. The device falls under product code DXJ (Display, Cathode-Ray Tube, Medical), a Class II device regulated under 21 CFR 870.2450. Sorin Group Deutschland GmbH has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 8, 2017
- Date Received
- February 15, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Display, Cathode-Ray Tube, Medical
- Device Class
- Class II
- Regulation Number
- 870.2450
- Review Panel
- CV
- Submission Type