| Primary Device ID | 00889024508453 |
| NIH Device Record Key | e3902e42-645e-4f08-9210-3a4432afe703 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Zimmer Persona Knee System |
| Version Model Number | 82-0153-150-00 |
| Catalog Number | 82-0153-150-00 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | 1 (800) 343-9500 |
| customerservice@zimmerbiomet.com |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024508453 [Primary] |
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
[00889024508453]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-10-15 |
| Device Publish Date | 2018-03-26 |