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

NANOVIS SPINAL SYSTEM

K Number: K113173 · Decision Jan 19, 2012
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
10
Review Days
84

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Basic Information

Device Name
NANOVIS SPINAL SYSTEM
K Number
K113173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nanovis, LLC
Date Received
October 27, 2011
Decision Date
January 19, 2012
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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K Number Device Name
K241605 Adaptix™ PEEK Interbody System with Nanotechnology; Capstone Control™ PEEK Spinal System with Nanotechnology
K230936 Anatomic PEEK™ Cervical Fusion System with Nanotechnology
K203452 Nano FortiFix® System
K191822 Nano FortiCore, FortiCore
K171312 FortiCore®
K161485 Nanovis Intervertebral Body Fusion System and Forticore(R)
K160874 Nanovis Intervertebral Body Fusion System and FortiCore®
K140280 FORTICORE
K110442 NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM