Primary Device ID | 00815362027370 |
NIH Device Record Key | 76d5b1bf-69fe-48e6-9c3c-084116de260e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reform Pedicle Screw System |
Version Model Number | 39-CC-0032 |
Catalog Number | 39-CC-0032 |
Company DUNS | 079398589 |
Company Name | PRECISION SPINE, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
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 |