| Primary Device ID | 00889024194410 |
| NIH Device Record Key | 3f510563-65e8-4ce3-9cfa-ca09ea711807 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5842-52-10 |
| Catalog Number | 00-5842-052-10 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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 |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Height | 10 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024194410 [Primary] |
| HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-10 |
| Device Publish Date | 2015-09-24 |
| 00889024681897 - Alliance | 2025-08-14 |
| 00889024681903 - Alliance | 2025-08-14 |
| 00889024681910 - Comprehensive | 2025-08-14 |
| 00889024681927 - Alliance | 2025-08-14 |
| 00889024681934 - Comprehensive | 2025-08-14 |
| 00889024681941 - Comprehensive | 2025-08-14 |
| 00889024681958 - Comprehensive | 2025-08-14 |
| 00889024681965 - Comprehensive | 2025-08-14 |