Primary Device ID | 00613994839305 |
NIH Device Record Key | f189d526-d342-4e57-8642-22eb4fb1d7a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vantage Anterior Fixation System |
Version Model Number | X0410352 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, 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 | 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 | +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 |
Length | 35 Millimeter |
Length | 35 Millimeter |
Length | 35 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 35 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994839305 [Primary] |
KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
[00613994839305]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-09 |
00613994839305 | BOLT X0410352 VAN TI 8X35 |
00613994839299 | BOLT X0410353 VAN TI 8X40 |
00613994839282 | BOLT X0410354 VAN TI 8X45 |
00613994839275 | BOLT X0410355 VAN TI 8X50 |
00613994839268 | BOLT X0410356 VAN TI 8X55 |
00613994839251 | BOLT X0410358 VAN TI 9X20 |
00613994839244 | BOLT X0410359 VAN TI 9X25 |
00613994839237 | BOLT X0410360 VAN TI 9X30 |
00613994839220 | BOLT X0410361 VAN TI 9X35 |
00613994839213 | BOLT X0410362 VAN TI 9X40 |
00613994839206 | BOLT X0410363 VAN TI 9X45 |
00613994839190 | BOLT X0410364 VAN TI 9X50 |
00613994839183 | BOLT X0410365 VAN TI 9X55 |