Primary Device ID | 00814729024922 |
NIH Device Record Key | 29b21b2c-352a-4e05-a962-345b55d1b2c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InFill Convex TLIF |
Version Model Number | 41-06-112815 |
Company DUNS | 962347980 |
Company Name | PINNACLE SPINE GROUP, LLC |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814729024922 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00814729024922]
Radiation Sterilization;Moist Heat or Steam Sterilization
[00814729024922]
Radiation Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2016-08-26 |
00814729025028 | 41-06-113016 |
00814729025011 | 41-06-113015 |
00814729025004 | 41-06-113014 |
00814729024991 | 41-06-113013 |
00814729024984 | 41-06-113012 |
00814729024977 | 41-06-113011 |
00814729024960 | 41-06-113010 |
00814729024953 | 41-06-113009 |
00814729024946 | 41-06-113008 |
00814729024939 | 41-06-112816 |
00814729024922 | 41-06-112815 |
00814729024915 | 41-06-112814 |
00814729024908 | 41-06-112813 |
00814729024892 | 41-06-112812 |
00814729024885 | 41-06-112811 |
00814729024878 | 41-06-112810 |
00814729024861 | 41-06-112809 |
00814729024854 | 41-06-112808 |