Persona® Natural Tibia™ 00-5907-081-04
GUDID 00889024203693
Zimmer, Inc.
Sterilization/disinfection container| Primary Device ID | 00889024203693 |
| NIH Device Record Key | 8fd0575c-8e71-43c6-94c9-488c6ba8af5e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Persona® Natural Tibia™ |
| Version Model Number | 00-5907-081-04 |
| Catalog Number | 00-5907-081-04 |
| 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 | true |
| Serial Number | false |
| 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 |
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 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 | 00889024203693 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K150090
FDA Product Code
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
[00889024203693]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-05-07 |
| Device Publish Date | 2016-08-10 |
On-Brand Devices [Persona® Natural Tibia™]
| 00889024203723 | 00-5907-081-07 |
| 00889024203716 | 00-5907-081-06 |
| 00889024203709 | 00-5907-081-05 |
| 00889024203693 | 00-5907-081-04 |
| 00889024203686 | 00-5907-081-03 |
| 00889024203679 | 00-5907-081-02 |
| 00889024203587 | 00-5907-080-92 |
| 00889024203570 | 00-5907-080-91 |
| 00889024203563 | 00-5907-080-90 |
| 00889024203556 | 00-5907-080-89 |
| 00889024203549 | 00-5907-080-88 |
| 00889024203532 | 00-5907-080-87 |
Trademark Results [Persona]
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