Bio-Modular® Shoulder System 113940
GUDID 00887868254000
Biomet Orthopedics, LLC
Shoulder glenoid fossa prosthesis, prefabricated| Primary Device ID | 00887868254000 |
| NIH Device Record Key | c5f8e46f-49dd-45af-bd04-5967454d5a87 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bio-Modular® Shoulder System |
| Version Model Number | 113940 |
| Catalog Number | 113940 |
| 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 | true |
| 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
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868254000 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K030710
FDA Product Code
| KWT | PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2018-07-23 |
On-Brand Devices [Bio-Modular® Shoulder System]
Trademark Results [Bio-Modular]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIO-MODULAR 73737260 1522520 Live/Registered |
BIOMET, INC. 1988-06-29 |
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