510(k) K171767
K171767 is an FDA 510(k) premarket notification submitted by Cianna Medical, Inc. for the device "Cianna Medical SAVI Scout Reflector and SAVI Scout System". The FDA issued a decision of Substantially Equivalent on October 31, 2017. The device falls under product code NEU (Marker, Radiographic, Implantable), a Class II device regulated under 21 CFR 878.4300. Cianna Medical, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 2017
- Date Received
- June 14, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Marker, Radiographic, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4300
- Review Panel
- SU
- Submission Type