NO-PROFILE 904428
GUDID 00880304405776
Biomet Sports Medicine, LLC
Ligament bone anchor| Primary Device ID | 00880304405776 |
| NIH Device Record Key | c4081b0e-f940-4033-9e89-763dfe7f6f17 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NO-PROFILE |
| Version Model Number | 904428 |
| Catalog Number | 904428 |
| Company DUNS | 627100159 |
| Company Name | Biomet Sports Medicine, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304405776 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
| HWC | Screw, fixation, bone |
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 | 2015-10-24 |
On-Brand Devices [NO-PROFILE]
| 00880304406155 | 904648 |
| 00880304406148 | 904646 |
| 00880304406131 | 904644 |
| 00880304406124 | 904642 |
| 00880304406117 | 904640 |
| 00880304406100 | 904638 |
| 00880304406094 | 904636 |
| 00880304406087 | 904634 |
| 00880304406070 | 904632 |
| 00880304406063 | 904630 |
| 00880304406056 | 904570 |
| 00880304406049 | 904565 |
| 00880304406032 | 904560 |
| 00880304406025 | 904555 |
| 00880304406018 | 904550 |
| 00880304406001 | 904545 |
| 00880304405998 | 904540 |
| 00880304405981 | 904535 |
| 00880304405974 | 904530 |
| 00880304405776 | 904428 |
Trademark Results [NO-PROFILE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NO-PROFILE 77405321 not registered Dead/Abandoned |
CSAV, Inc. 2008-02-25 |
 NO-PROFILE 74365131 1846562 Dead/Cancelled |
Stow-Away Controls, Inc. 1993-03-05 |
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