Primary Device ID | 00190837011192 |
NIH Device Record Key | c9738f28-bbf5-4aa0-80c9-501b9e194c39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Plateau-A Anterior Lumbar Spacer System |
Version Model Number | 64-3428-613 |
Company DUNS | 183641617 |
Company Name | Life Spine, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | 00190837011192 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837011192]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2016-06-20 |
00190837011222 | 64-3428-619 |
00190837011215 | 64-3428-617 |
00190837011208 | 64-3428-615 |
00190837011192 | 64-3428-613 |
00190837011185 | 64-3428-611 |
00190837011178 | 64-3428-609 |
00190837011161 | 64-3428-1219 |
00190837011154 | 64-3428-1217 |
00190837011147 | 64-3428-1215 |
00190837011130 | 64-3428-1213 |
00190837011123 | 64-3428-1211 |
00190837011116 | 64-3428-1209 |
00190837011109 | 64-3024-619 |
00190837011093 | 64-3024-617 |
00190837011086 | 64-3024-615 |
00190837011079 | 64-3024-613 |
00190837011062 | 64-3024-611 |
00190837011055 | 64-3024-609 |
00190837011048 | 64-3024-1219 |
00190837011031 | 64-3024-1217 |
00190837011024 | 64-3024-1215 |
00190837011017 | 64-3024-1213 |
00190837011000 | 64-3024-1211 |
00190837010997 | 64-3024-1209 |