| Primary Device ID | 00887868115660 |
| NIH Device Record Key | 4880ff75-be69-490a-bd98-c03671440734 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FRS™ SCREW |
| Version Model Number | P1032 |
| Catalog Number | P1032 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, 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)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868115660 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
[00887868115660]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00887868115752 | P2016 |
| 00887868115745 | P2014 |
| 00887868115738 | P2012 |
| 00887868115721 | P2010 |
| 00887868115677 | P1034 |
| 00887868115660 | P1032 |
| 00887868115653 | P1030 |
| 00887868115646 | P1028 |
| 00887868115639 | P1026 |
| 00887868115622 | P1024 |
| 08426750013886 | P2026 |
| 08426750013879 | P2024 |
| 08426750013862 | P2022 |
| 08426750013855 | P2020 |
| 08426750013848 | P2018 |