Prolift Post-Pack Instruments 151-275

GUDID 00190837031879

Life Spine, Inc.

Metallic spinal interbody fusion cage
Primary Device ID00190837031879
NIH Device Record Keya550637c-341e-4d98-8ecc-d5112031c9ed
Commercial Distribution StatusIn Commercial Distribution
Brand NameProlift Post-Pack Instruments
Version Model Number151-275
Catalog Number151-275
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 Usefalse
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
GS100190837031879 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190837031879]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2019-11-07

On-Brand Devices [Prolift Post-Pack Instruments]

00190837032111151-302
00190837032104151-299
00190837032098151-296
00190837031978151-285
00190837031961151-281
00190837031954151-279
00190837031947151-276
00190837031930151-273
00190837031923151-270
00190837031916151-267
00190837031909151-264
00190837031893151-284
00190837031886151-278
00190837031879151-275
00190837031862151-272
00190837031855151-269
00190837031848151-266
00190837031831151-263
00190837031824129-518
00190837031817129-517
00190837031800129-516
00190837031794129-515
00190837031787129-514
00190837031770129-513
00190837031763129-512
00190837031756129-511
00190837031282151-295

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