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

FOCUS Pedicle Screw System

K Number: K180458 · Decision Apr 17, 2018
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
10
Review Days
56

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Basic Information

Device Name
FOCUS Pedicle Screw System
K Number
K180458
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nvision Biomedical Technologies, LLC
Date Received
February 20, 2018
Decision Date
April 17, 2018
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

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