The following data is part of a premarket notification filed by Cianna Medical, Inc. with the FDA for Cianna Medical Savi Scout Reflector And Savi Scout System.
Device ID | K171767 |
510k Number | K171767 |
Device Name: | Cianna Medical SAVI Scout Reflector And SAVI Scout System |
Classification | Marker, Radiographic, Implantable |
Applicant | Cianna Medical, Inc. 6 Journey, Suite 125 Aliso Viejo, CA 92656 |
Contact | Gary Mocnik |
Correspondent | Gary Mocnik Cianna Medical, Inc. 6 Journey, Suite 125 Aliso Viejo, CA 92656 |
Product Code | NEU |
CFR Regulation Number | 878.4300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-14 |
Decision Date | 2017-10-31 |