| Primary Device ID | 00814729024977 |
| NIH Device Record Key | 499c60f5-148c-473d-867d-e347a07673a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InFill Convex TLIF |
| Version Model Number | 41-06-113011 |
| 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 | 00814729024977 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00814729024977]
Radiation Sterilization;Moist Heat or Steam Sterilization
[00814729024977]
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 |