| Primary Device ID | 03760297030117 |
| NIH Device Record Key | 59e9c231-baac-49dd-8247-6ab813e5813d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KneePlus |
| Version Model Number | Knee+ |
| Catalog Number | KNS002 |
| Company DUNS | 270195749 |
| Company Name | PIXEE MEDICAL |
| 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 | true |
| 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 | 03760297030117 [Primary] |
| OLO | Orthopedic Stereotaxic Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-18 |
| Device Publish Date | 2021-10-08 |
| 03760297030117 | Software for Total Knee Arthroplasty |
| 03760297030124 | Software for Total Knee Arthroplasty |
| 03760297030315 | Software for Total Knee Arthroplasty |
| 03760297030469 | Software for Total Knee Arthroplasty |