Primary Device ID | 04712602349017 |
NIH Device Record Key | 26ccb5e4-65f7-436a-9b22-e0deceb5e6e5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Femoral augment, Posterior |
Version Model Number | 2603-5041 |
Catalog Number | 2603-5041 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
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 |
04712771480177 | Femoral augment, Posterior, #6, 8mm |
04712771480160 | Femoral augment, Posterior, #6, 4mm |
04712602349048 | Femoral augment, Posterior, #5, 8mm |
04712602349031 | Femoral augment, Posterior, #5, 4mm |
04712602349024 | Femoral augment, Posterior, #4, 8mm |
04712602349017 | Femoral augment, Posterior, #4, 4mm |
04712602349000 | Femoral augment, Posterior, #3, 8mm |
04712602348997 | Femoral augment, Posterior, #3, 4mm |
04712602348980 | Femoral augment, Posterior, #2, 8mm |
04712602348973 | Femoral augment, Posterior, #2, 4mm |
04712602348966 | Femoral augment, Posterior, #1, 8mm |
04712602348959 | Femoral augment, Posterior, #1, 4mm |