| Primary Device ID | 00880304830301 |
| NIH Device Record Key | ffa29e1e-e069-4d71-9896-d94223249465 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM |
| Version Model Number | 8616-4512 |
| Catalog Number | 8616-4512 |
| 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 |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com | |
| Phone | +1(800)447-3625 |
| USBROCustomerService@zimmerbiomet.com |
| 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 | 00880304830301 [Primary] |
| MWP | Cabinet,x-ray system |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
Moist Heat or Steam Sterilization
[00880304830301]
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 |