Primary Device ID | 00628184008157 |
NIH Device Record Key | 1c7f5b79-a799-4614-ad6b-a59d409ea829 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | intellijoint KNEE (R) |
Version Model Number | 000-0815 |
Company DUNS | 202958070 |
Company Name | Intellijoint Surgical Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |