Primary Device ID | 00190837079475 |
NIH Device Record Key | 70277b68-38a0-4246-9167-49d61b1a75f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ZB ProLift Narrow |
Version Model Number | 58-1228-1208Z |
Catalog Number | 58-1228-1208Z |
Company DUNS | 183641617 |
Company Name | Life Spine, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190837079475 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-11-07 |
00190837079505 | 58-1228-1510Z |
00190837079499 | 58-1228-1508Z |
00190837079482 | 58-1228-1210Z |
00190837079475 | 58-1228-1208Z |
00190837079468 | 58-1228-1016Z |
00190837079451 | 58-1228-0813Z |
00190837079444 | 58-1228-0710Z |
00190837079437 | 58-1228-0708Z |
00190837079420 | 58-1028-1510Z |
00190837079413 | 58-1028-1508Z |
00190837079406 | 58-1028-1210Z |
00190837079390 | 58-1028-1208Z |
00190837079383 | 58-1028-1016Z |
00190837079376 | 58-1028-0813Z |
00190837079369 | 58-1028-0710Z |
00190837079352 | 58-1028-0708Z |
00190837079345 | 151-567 |
00190837079338 | 151-565 |
00190837079321 | 151-512 |
00190837079314 | 151-510 |
00190837079307 | 151-457 |
00190837079291 | 151-455 |
00190837079284 | 151-402 |
00190837079277 | 151-400 |