Primary Device ID | 00819824022590 |
NIH Device Record Key | 97e027d3-9b58-4d80-8d2f-3c54061e3fa4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XULTAN 5.5 REDUCTION PEDICLE SCREW 7.5 X 65 MM CANN |
Version Model Number | 51756500 |
Catalog Number | 51756500 |
Company DUNS | 080474650 |
Company Name | MET 1 TECHNOLOGIES, LLC |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 9154726762 |
yone@met1tech.com | |
Phone | 9154726762 |
yone@met1tech.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00819824022590 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00819824022590]
Moist Heat or Steam Sterilization
[00819824022590]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-03-29 |
00819824022729 | THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLANT DEVICE MANUFACTURED FROM TITANIUM AND SILICONE |
00819824022590 | THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLANT DEVICE MANUFACTURED FROM TITANIUM AND SILICONE |