NEO / Kinetic Anterior Cervical Plate System

GUDID 00190837005122

Life Spine, Inc.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00190837005122
NIH Device Record Key182fac3a-d4c1-4ee7-80f0-54e3335ec0c6
Commercial Distribution StatusIn Commercial Distribution
Brand NameNEO / Kinetic Anterior Cervical Plate System
Version Model Number202-014
Company DUNS183641617
Company NameLife Spine, Inc.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837005122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


[00190837005122]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-13

On-Brand Devices [NEO / Kinetic Anterior Cervical Plate System]

00190837005191203-018
00190837005184203-016
00190837005177203-014
00190837005160203-012
00190837005153203-010
00190837005146202-018
00190837005139202-016
00190837005122202-014
00190837005115202-012
00190837005108202-010
00190837005092201-018
00190837005085201-016
00190837005078201-014
00190837005061201-012
00190837005054201-010
00190837004736111-001
00190837004729103-018
00190837004712103-016
00190837004705103-014
00190837004699103-012
00190837004682103-010
00190837004675102-018
00190837004668102-016
00190837004651102-014
00190837004644102-012
00190837004637102-010
00190837004620101-018
00190837004613101-016
00190837004606101-014
00190837004590101-012
00190837004583101-010
00190837036775Neo Fixed Angle Drill Guide
00190837036805Kinetic Single-Barrel Clip-On Fixed Angle Drill Guide
00190837036799Kinetic Fixed Angle Drill Guide
00190837036782Kinetic Distractor Clip
0019083703676814mm Fixation Pin
00190837036751MIS CT Handle
00190837036744Custom Screw Caddy, NEO / Kinetic
00190837036737Custom Locking Bone Screw Driver
00190837036720Single Barrel Fixed Angle Drill Guide (Left)
00190837036713Single Barrel Fixed Angle Drill Guide (Right)
00190837036706Locking Fixation Pin Driver
00190837036690Sleeved Screw Driver
00190837036683Fluted Fixation Pin
00190837036676Drill Guide
00190837036669Kinetic-Iris 2-Level, 44mm
00190837036652KINETIC SL Dynamic Distractor Clip, 1.6mm (PEEK)
001908370366452mm KINETIC SL Distractor
001908370366381mm KINETIC Distractor
00190837036621NEO / KINETIC FT Screw Caddy

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.