| Primary Device ID | 00889024167483 |
| NIH Device Record Key | ade1b5eb-f3a9-4526-a958-b532802e875a |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 4364-32-067 |
| Catalog Number | 4364-32-067 |
| 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 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024167483 [Primary] |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-14 |
| Device Publish Date | 2017-10-23 |
| 00887868585654 - Zimmer Biomet® 12/14 Spherical Head Trials | 2024-11-13 |
| 00889024630192 - Persona® Knee System | 2024-11-13 |
| 00889024630208 - Persona® Knee System | 2024-11-13 |
| 00889024630215 - Persona® Knee System | 2024-11-13 |
| 00889024630222 - Persona® Knee System | 2024-11-13 |
| 00889024630239 - Persona® Knee System | 2024-11-13 |
| 00889024630246 - Persona® Knee System | 2024-11-13 |
| 00889024630253 - Persona® Knee System | 2024-11-13 |