| Primary Device ID | 00814289020433 |
| NIH Device Record Key | 8879f863-e2e1-45ba-b50c-39ffecdaedd6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Conventus Cage - Plate |
| Version Model Number | PX01 |
| Company DUNS | 021231299 |
| Company Name | CONVENTUS ORTHOPAEDICS, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | false |
| 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 | 00814289020433 [Primary] |
| HSB | Rod, Fixation, Intramedullary And Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00814289020433]
Moist Heat or Steam Sterilization
[00814289020433]
Moist Heat or Steam Sterilization
[00814289020433]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-09-18 |