ZB ProLift Narrow 58-1228-0710Z

GUDID 00190837079444

Life Spine, Inc.

Metallic spinal interbody fusion cage
Primary Device ID00190837079444
NIH Device Record Keyb9fb8fa0-0c60-4f34-9f9a-f7862dd69d26
Commercial Distribution StatusIn Commercial Distribution
Brand NameZB ProLift Narrow
Version Model Number58-1228-0710Z
Catalog Number58-1228-0710Z
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 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
GS100190837079444 [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 StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2019-11-07

On-Brand Devices [ZB ProLift Narrow]

0019083707950558-1228-1510Z
0019083707949958-1228-1508Z
0019083707948258-1228-1210Z
0019083707947558-1228-1208Z
0019083707946858-1228-1016Z
0019083707945158-1228-0813Z
0019083707944458-1228-0710Z
0019083707943758-1228-0708Z
0019083707942058-1028-1510Z
0019083707941358-1028-1508Z
0019083707940658-1028-1210Z
0019083707939058-1028-1208Z
0019083707938358-1028-1016Z
0019083707937658-1028-0813Z
0019083707936958-1028-0710Z
0019083707935258-1028-0708Z
00190837079345151-567
00190837079338151-565
00190837079321151-512
00190837079314151-510
00190837079307151-457
00190837079291151-455
00190837079284151-402
00190837079277151-400

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