Primary Device ID | 00850007069124 |
NIH Device Record Key | 228ebdab-21dc-4a06-a712-34aaca222e92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MaxView™ System - Posterior Set |
Version Model Number | VSY-2060 |
Company DUNS | 096680671 |
Company Name | VISEON, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
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00850007069216 | Spinal access and visualization system, 26mm diameter, 50mm length |
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00850007069063 | Spinal access and visualization system, 18mm diameter, 50mm length |
00850007069056 | Spinal access and visualization system, 18mm diameter, 40mm length |
00850007069049 | Spinal access and visualization system, 16mm diameter, 80mm length |
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00850007069025 | Spinal access and visualization system, 16mm diameter, 60mm length |
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