Arcos® STS™ Modular Revision System 31-300866
GUDID 00887868475610
Biomet Orthopedics, LLC
Bone-resection orthopaedic reamer, reusable| Primary Device ID | 00887868475610 |
| NIH Device Record Key | 47311392-921c-4821-81a7-366da5ceabfd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arcos® STS™ Modular Revision System |
| Version Model Number | 31-300866 |
| Catalog Number | 31-300866 |
| 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 | 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 |
Customer Support Contacts
Device Dimensions
| 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 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868475610 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K100469
FDA Product Code
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
[00887868475610]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-06-02 |
| Device Publish Date | 2022-05-25 |
On-Brand Devices [Arcos® STS™ Modular Revision System]
Trademark Results [Arcos]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ARCOS 98679915 not registered Live/Pending |
Dosamar Corporation 2024-08-02 |
 ARCOS 98001041 not registered Live/Pending |
HLI Solutions, Inc. 2023-05-17 |
 ARCOS 97567037 not registered Live/Pending |
Siman, Alvaro E. 2022-08-26 |
 ARCOS 97141919 not registered Live/Pending |
Hubbell Lighting, Inc. 2021-11-24 |
 ARCOS 88750745 not registered Live/Pending |
Arcos, Inc. 2020-01-08 |
 ARCOS 88500444 not registered Live/Pending |
Archimedes Controls Corp. 2019-07-03 |
 ARCOS 87601803 5577107 Live/Registered |
Arrcus, Inc. 2017-09-08 |
 ARCOS 87588350 not registered Dead/Abandoned |
SCOPERTA IMPORTING COMPANY 2017-08-29 |
 ARCOS 86823144 5392314 Live/Registered |
Dosamar Corporation 2015-11-17 |
 ARCOS 86114301 not registered Dead/Abandoned |
Smith, Logan 2013-11-08 |
 ARCOS 85801573 4379613 Live/Registered |
ARCOS, LLC 2012-12-13 |
 ARCOS 85801564 4379612 Live/Registered |
ARCOS, LLC 2012-12-13 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.