ProLift Expandable Spacer System Post Pack

GUDID 00190837022747

Life Spine, Inc.

Metallic spinal fusion cage, non-sterile
Primary Device ID00190837022747
NIH Device Record Keycbaef816-ecf8-4ea0-9729-530831e3ee0c
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLift Expandable Spacer System Post Pack
Version Model Number58-1228-1016D
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
GS100190837022747 [Primary]

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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-17
Device Publish Date2018-11-14

On-Brand Devices [ProLift Expandable Spacer System Post Pack]

0019083702274758-1228-1016D
0019083702273058-1228-0813D
0019083702160358-1228-1016P
0019083702159758-1228-1208D
0019083702158058-1228-0710D
0019083702157358-1228-0708D

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