ProLift Lateral Fixated

GUDID 00190837101435

Life Spine, Inc.

Metallic spinal interbody fusion cage
Primary Device ID00190837101435
NIH Device Record Key6b9be433-dfab-4457-97ee-1a5b09968606
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLift Lateral Fixated
Version Model Number58-2255-0710LP
Company DUNS183641617
Company NameLife Spine, 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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837101435 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


[00190837101435]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-06-08
Device Publish Date2022-05-31

On-Brand Devices [ProLift Lateral Fixated]

0019083710112158-1850-0708LP
0019083710111458-1850-0010LP
0019083710110758-1850-0008LP
0019083710113858-1850-0710LP
0019083710119058-1855-0710LP
0019083710124458-1860-0708LP
0019083710106058-1845-0708LP
0019083710121358-1855-1512LP
0019083710120658-1855-1510LP
0019083710118358-1855-0708LP
0019083710117658-1855-0010LP
0019083710116958-1855-0008LP
0019083710115258-1850-1512LP
0019083710114558-1850-1510LP
0019083710109158-1845-1512LP
0019083710108458-1845-1510LP
0019083710107758-1845-0710LP
0019083710105358-1845-0010LP
0019083710104658-1845-0008LP
0019083710141158-2255-0010LP
0019083710140458-2255-0008LP
0019083710139858-2250-1513LP
0019083710138158-2250-1511LP
0019083710137458-2250-0710LP
0019083710136758-2250-0708LP
0019083710135058-2250-0010LP
0019083710134358-2250-0008LP
0019083710133658-2245-1513LP
0019083710132958-2245-1511LP
0019083710131258-2245-0710LP
0019083710130558-2245-0708LP
0019083710129958-2245-0010LP
0019083710128258-2245-0008LP
0019083710127558-1860-1512LP
0019083710126858-1860-1510LP
0019083710125158-1860-0710LP
0019083710123758-1860-0010LP
0019083710122058-1860-0008LP
0019083710151058-2260-1513LP
0019083710150358-2260-1511LP
0019083710149758-2260-0710LP
0019083710148058-2260-0708LP
0019083710147358-2260-0010LP
0019083710146658-2260-0008LP
0019083710145958-2255-1513LP
0019083710144258-2255-1511LP
0019083710143558-2255-0710LP
0019083710142858-2255-0708LP

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