LxHA™ LXL22126000

GUDID M711LXL221260001

HA PEEK, Ta

Innovasis, Inc.

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage
Primary Device IDM711LXL221260001
NIH Device Record Key6483487a-ed81-4f4a-9028-81184835230d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLxHA™
Version Model NumberLXL22126000
Catalog NumberLXL22126000
Company DUNS156567492
Company NameInnovasis, Inc.
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

Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com
Phone801-261-2236
Emailinfo@innovasis.com

Device Dimensions

Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree
Width22 Millimeter
Height12 Millimeter
Length60 Millimeter
Angle0 degree

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM711LXL221260000 [Primary]
HIBCCM711LXL221260001 [Package]
Contains: M711LXL221260000
Package: Carton [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-10-20
Device Publish Date2019-07-31

On-Brand Devices [LxHA™]

M711LS5080SST, Silicone, Al, Adhesive
M711LS463240SST
M711LS463180SST
M711BTA1730Cross-linked Polyethylene, Convoluted Polyurethane, Lexan
M711BTA1710Al, SST, Nylon, Silicone, Radel
M711BTA1700Al, SST, Nylon, Silicone, Radel
M711LXL181250121HA PEEK, Ta
M711LXL181250081HA PEEK, Ta
M711LXL181250001HA PEEK, Ta
M711LXL181245161HA PEEK, Ta
M711LXL181245121HA PEEK, Ta
M711LXL181245081HA PEEK, Ta
M711LXL181245001HA PEEK, Ta
M711LXL181060121HA PEEK, Ta
M711LXL181060081HA PEEK, Ta
M711LXL181060001HA PEEK, Ta
M711LXL181055121HA PEEK, Ta
M711LXL181055081HA PEEK, Ta
M711LXL181055001HA PEEK, Ta
M711LXL181050121HA PEEK, Ta
M711LXL181050081HA PEEK, Ta
M711LXL181050001HA PEEK, Ta
M711LXL181045081HA PEEK, Ta
M711LXL181045001HA PEEK, Ta
M711LXL180860081HA PEEK, Ta
M711LXL180860001HA PEEK, Ta
M711LXL180855081HA PEEK, Ta
M711LXL180855001HA PEEK, Ta
M711LXL180850081HA PEEK, Ta
M711LXL180850001HA PEEK, Ta
M711LXL180845081HA PEEK, Ta
M711LXL180845001HA PEEK, Ta
M711LXL261655161HA PEEK, Ta
M711LXL261655121HA PEEK, Ta
M711LXL261655081HA PEEK, Ta
M711LXL261655001HA PEEK, Ta
M711LXL261650161HA PEEK, Ta
M711LXL261650121HA PEEK, Ta
M711LXL261650081HA PEEK, Ta
M711LXL261650001HA PEEK, Ta
M711LXL261645161HA PEEK, Ta
M711LXL261645121HA PEEK, Ta
M711LXL261645081HA PEEK, Ta
M711LXL261645001HA PEEK, Ta
M711LXL261460161HA PEEK, Ta
M711LXL261460121HA PEEK, Ta
M711LXL261460081HA PEEK, Ta
M711LXL261460001HA PEEK, Ta
M711LXL261455161HA PEEK, Ta
M711LXL261455121HA PEEK, Ta

Trademark Results [LxHA]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LXHA
LXHA
88127521 not registered Live/Pending
Innovasis, Inc.
2018-09-21
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