ProLift Lateral 149-1410

GUDID 00190837085681

Lateral Trial Inserter, Angled, 15 Degree

Life Spine, Inc.

Metallic spinal fusion cage, sterile
Primary Device ID00190837085681
NIH Device Record Key05d0addf-148f-4c50-ae11-15baab17bb31
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLift Lateral
Version Model Number149-1410
Catalog Number149-1410
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
GS100190837085681 [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

[00190837085681]

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 [ProLift Lateral]

00190837098223149-898
00190837096359149-1032
00190837096342149-1031
00190837096335149-1030
00190837096328149-1029
00190837096311149-1028
00190837096304149-1027
00190837096298149-1025
00190837096281149-1023
00190837095390149-1026
00190837095383149-1024
00190837095376149-1022
00190837094539149-796
00190837094522149-795
00190837094515149-794
00190837094508149-793
00190837094492149-792
00190837094485149-791
00190837094478149-789
00190837094461149-787
00190837094454149-785
00190837094447149-784
00190837094430149-779
00190837094423149-778
00190837094416149-777
00190837094409149-776
00190837094393149-774
00190837094386149-773
00190837094379149-772
00190837094362149-771
00190837094355149-770
00190837094348149-769
00190837094331149-767
00190837094324149-766
00190837094317149-765
00190837094300149-764
00190837094294149-763
00190837094287149-762
00190837094270149-761
00190837094263149-760
00190837094256149-759
00190837094249149-758
00190837094232149-757
00190837094225149-756
00190837094218149-755
00190837094201149-754
00190837094195149-753
00190837094188149-752
00190837094171149-751
00190837094164149-750

© 2019 FDA.report
This site is not affiliated with or endorsed by the FDA.