| Primary Device ID | 00887868252006 |
| NIH Device Record Key | 24a0ce1c-40b6-4f0c-9fe4-ee773811d41f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | JuggerKnot® Soft Anchors |
| Version Model Number | 912075 |
| Catalog Number | 912075 |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868252006 [Primary] |
| MBI | Fastener, fixation, nondegradable, soft tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-05-05 |
| Device Publish Date | 2018-09-14 |
| 00880304858992 - JUGGERKNOT | 2025-09-22 |
| 00880304404809 - MINI RC NEEDLE | 2025-09-08 |
| 00887868571718 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571725 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571732 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571749 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571756 - RingLoc®+ Triflange | 2025-06-20 |
| 00887868571763 - RingLoc®+ Triflange | 2025-06-20 |
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 |