JUGGERKNOT® 110025769
GUDID 00880304685291
Biomet Orthopedics, LLC
Ligament bone anchor| Primary Device ID | 00880304685291 |
| NIH Device Record Key | b830ffe7-363b-4308-b74e-fdd474e5d040 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | JUGGERKNOT® |
| Version Model Number | 110025769 |
| Catalog Number | 110025769 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | 00880304685291 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K150768
FDA Product Code
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-01-08 |
| Device Publish Date | 2016-04-05 |
On-Brand Devices [JUGGERKNOT®]
Trademark Results [JUGGERKNOT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 JUGGERKNOT 97275055 not registered Live/Pending |
Hong, Charles 2022-02-18 |
 JUGGERKNOT 86111740 4555637 Live/Registered |
Biomet Sports Medicine, LLC 2013-11-06 |
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