Nex-Link OCT® 7002-01

GUDID 00889024337862

BIOMET SPINE LLC

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00889024337862
NIH Device Record Keyd79be518-4fcf-4f6d-a2e1-8f3df217050c
Commercial Distribution StatusIn Commercial Distribution
Brand NameNex-Link OCT®
Version Model Number7002-01
Catalog Number7002-01
Company DUNS018577570
Company NameBIOMET SPINE LLC
Device Count1
DM Exemptfalse
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

Customer Support Contacts

Phone+1(800)447-3625
Email[email protected]

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024337862 [Primary]

FDA Product Code

KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024337862]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-27
Device Publish Date2019-11-19

On-Brand Devices [Nex-Link OCT®]

008890243324092115-4052
008890243323932115-4050
008890243323862115-4048
008890243323792115-4046
008890243323622115-4044
008890243323552115-4042
008890243323482115-4040
008890243378627002-01
008890243378557001-01

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