FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

GALAXY MIS Screw System

K Number: K143110 · Decision Jun 24, 2015
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
1
Review Days
238

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
GALAXY MIS Screw System
K Number
K143110
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bm Korea
Date Received
October 29, 2014
Decision Date
June 24, 2015
Product Code
NKB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
NKB Thoracolumbosacral Pedicle Screw System

Similar 510(k) Clearances

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

View all