ProLift 151-627

GUDID 00190837105921

Static Expandable Cage Trial, 12mm x 28mm x 11mm, 12 Degree

Life Spine, Inc.

Metallic spinal fusion cage, sterile
Primary Device ID00190837105921
NIH Device Record Key345604f8-a89b-49a9-a44b-53ba97b9e18e
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLift
Version Model Number151-627
Catalog Number151-627
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
GS100190837105921 [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

[00190837105921]

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]

00190837093365149-781
00190837093358149-429
00190837093341151-1018
00190837093334151-1017
00190837093327151-1016
00190837093310149-780
00190837093303112-428
00190837093297112-427
00190837093280114-204-31
00190837093273114-204-21
00190837093266112-365
00190837091392149-4000
00190837090999151-301
00190837090968151-304
00190837090951151-303
00190837090944151-300
00190837090937151-298
00190837090920151-297
00190837090913151-282
0019083708670158-1228-1510K
0019083708669558-1228-1508K
0019083708668858-1228-1210K
0019083708667158-1228-1208K
0019083708666458-1228-1016K
0019083708665758-1228-0813K
0019083708664058-1228-0710K
0019083708663358-1228-0708K
0019083708662658-1032-1510K
0019083708661958-1032-1508K
0019083708660258-1032-1210K
0019083708659658-1032-1208K
0019083708658958-1032-1016K
0019083708657258-1032-0813K
0019083708656558-1032-0710K
0019083708655858-1032-0708K
0019083708654158-1028-1510K
0019083708653458-1028-1508K
0019083708652758-1028-1210K
0019083708651058-1028-1208K
0019083708650358-1028-1016K
0019083708649758-1028-0813K
0019083708648058-1028-0710K
0019083708647358-1028-0708K
0019083708646658-0828-1510K
0019083708645958-0828-1508K
0019083708644258-0828-1210K
0019083708643558-0828-1208K
0019083708642858-0828-1016K
0019083708641158-0828-0813K
0019083708640458-0828-0710K

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