| Primary Device ID | 00880304678767 |
| NIH Device Record Key | 4a1eb3f1-8481-47ad-a4eb-adde973319cb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OSS STRAIGHT STEM TRIAL |
| Version Model Number | 110018691 |
| Catalog Number | 110018691 |
| 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 | false |
| 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 | 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 |
| 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 | 00880304678767 [Primary] |
| KRO | PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
[00880304678767]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-10-27 |
| 00880304679009 | 110018715 |
| 00880304678996 | 110018714 |
| 00880304678989 | 110018713 |
| 00880304678859 | 110018700 |
| 00880304678842 | 110018699 |
| 00880304678835 | 110018698 |
| 00880304678828 | 110018697 |
| 00880304678811 | 110018696 |
| 00880304678804 | 110018695 |
| 00880304678798 | 110018694 |
| 00880304678781 | 110018693 |
| 00880304678774 | 110018692 |
| 00880304678767 | 110018691 |
| 00880304678750 | 110018690 |
| 00880304678743 | 110018689 |
| 00880304678736 | 110018688 |
| 00880304678729 | 110018687 |
| 00880304678712 | 110018686 |
| 00880304678705 | 110018685 |
| 00880304678699 | 110018684 |
| 00880304678682 | 110018683 |
| 00880304678675 | 110018682 |