| Primary Device ID | 00880304830370 |
| NIH Device Record Key | d19e0cc8-f968-4516-8be6-337f4caff317 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM |
| Version Model Number | 8616-5016 |
| Catalog Number | 8616-5016 |
| Company DUNS | 018577570 |
| Company Name | BIOMET SPINE 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 | 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304830370 [Primary] |
| MAX | Intervertebral fusion device with bone graft, lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
[00880304830370]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-10-14 |