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

NuVasive® Camber Laminoplasty System

K Number: K191169 · Decision Jul 3, 2019
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
28
Applicant Total
73
Review Days
63

Basic Information

Device Name
NuVasive® Camber Laminoplasty System
K Number
K191169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NuVasive, Incorporated
Date Received
May 1, 2019
Decision Date
July 3, 2019
Product Code
NQW
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
NQW Orthosis, Spine, Plate, Laminoplasty, Metal

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Other Clearances by NuVasive, Incorporated

K Number Device Name
K231735 NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody System
K230894 NuVasive Modulus ALIF System
K230989 Rod Registration Frame
K223181 NuVasive Reline System
K221751 NuVasive Cohere ALIF System Intervertebral Body Fusion Device
K221388 NuVasive Reline Cervical System
K220478 NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody System
K213654 NuVasive Reline Cervical System
K203714 NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent Thoracolumbar System, NuVasive CoRoent XL Interfixated System, Brigade System, Brigade Lateral System, BASE Interfixated Titanium System, Coalesce Thoracolumbar Interbody Fusion System, NuVasive Cohere Thoracolumbar Interbody System, NuVasive Modulus XLIF Interbody System, NuVasive Modulus TLIF Interbody System, NuVasive Modulus ALIF System, NuVasive Attrax Putty
K212446 NuVasive Anterior Cervical Plate Systems
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