Primary Device ID | 00643169677913 |
NIH Device Record Key | 92307fce-834a-432e-b1b3-3a6702099012 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Capstone Control Spinal System |
Version Model Number | 4031722 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Height | 17 Millimeter |
Height | 17 Millimeter |
Height | 17 Millimeter |
Height | 17 Millimeter |
Height | 17 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Angle | 24 degree |
Length | 22 Millimeter |
Height | 17 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169677913 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-02 |
Device Publish Date | 2018-09-01 |
00643169677920 | SPACER 4031822 CONTROL 24 DEG 18X22 |
00643169677913 | SPACER 4031722 CONTROL 24 DEG 17X22 |
00643169677906 | SPACER 4031622 CONTROL 24 DEG 16X22 |
00643169677890 | SPACER 4031522 CONTROL 24 DEG 15X22 |
00643169677883 | SPACER 4031422 CONTROL 24 DEG 14X22 |
00643169677876 | SPACER 4031322 CONTROL 24 DEG 13X22 |
00643169674806 | SPACER 4031527 CONTROL 24 DEG 15X27 |