| Primary Device ID | 00880304459854 |
| NIH Device Record Key | efe67470-f890-4b12-84fb-73789914f93f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HYBRID GLENOID |
| Version Model Number | PT-113950 |
| Catalog Number | PT-113950 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304459854 [Primary] |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2015-10-24 |
| 00880304462625 | 113952 |
| 00880304462618 | 113956 |
| 00880304462489 | 113954 |
| 00880304462472 | 113951 |
| 00880304459854 | PT-113950 |
| 00880304456600 | 406152 |
| 00880304456587 | 406151 |
| 00880304456570 | 406182 |
| 00880304456457 | 406181 |
| 00880304456365 | 406150 |
| 00887868343865 | 113951 |
| 00887868261169 | SSI002443 |
| 00887868261152 | SSI002442 |