FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Cianna Medical SAVI Scout Reflector and SAVI Scout System

K Number: K181007 · Decision Aug 2, 2018
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
8
Review Days
107

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Cianna Medical SAVI Scout Reflector and SAVI Scout System
K Number
K181007
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cianna Medical, Inc.
Date Received
April 17, 2018
Decision Date
August 2, 2018
Product Code
NEU
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NEU Marker, Radiographic, Implantable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEU), ordered by most recent decision date.

View all

Other Clearances by Cianna Medical, Inc.

K Number Device Name
K171767 Cianna Medical SAVI Scout Reflector and SAVI Scout System
K161507 Cianna Medical SAVI Scout Reflector and SAVI Scout System
K141318 CIANNA MEDICAL SGS SYSTEM
K132463 CIANNA MEDICAL PERMANENT TISSUE MARKER AND DELIVERY SYSTEM
K101411 SAVI PREPARATION DEVICE
K081677 SAVI APPLICATOR KIT
K080565 MODIFICATION TO: SAVI APPLICATOR KIT