Primary Device ID | 00613994916136 |
NIH Device Record Key | a36fc1a1-d629-4254-a724-c0e0759b2cf5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PERIMETER® Interbody Fusion Device |
Version Model Number | X0910097 |
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 |
Length | 21 Millimeter |
Length | 21 Millimeter |
Length | 21 Millimeter |
Length | 21 Millimeter |
Length | 21 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Height | 18 Millimeter |
Width | 26 Millimeter |
Length | 21 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994916136 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
[00613994916136]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2015-06-29 |
00613994916341 | SPACER X0910108 PER TI LG 8D 30X12 |
00613994916334 | SPACER X0910109 PER TI LG 8D 30X14 |
00613994916327 | SPACER X0910110 PER TI LG 8D 30X16 |
00613994916310 | SPACER X0910111 PER TI LG 8D 30X18 |
00613994916303 | SPACER X0910112 PER TI LG 8D 30X20 |
00613994916297 | SPACER X0910113 PER TI LG 12D 30X8 |
00613994916280 | SPACER X0910114 PER TI LG 12D 30X10 |
00613994916273 | SPACER X0910115 PER TI LG 12D 30X12 |
00613994916266 | SPACER X0910116 PER TI LG 12D 30X14 |
00613994916259 | SPACER X0910117 PER TI LG 12D 30X16 |
00613994916242 | SPACER X0910118 PER TI LG 12D 30X18 |
00613994916235 | SPACER X0910119 PER TI LG 12D 30X20 |
00613994916228 | SPACER X0910120 PER TI XL 8D 36X8 |
00613994916211 | SPACER X0910121 PER TI XL 8D 36X10 |
00613994916204 | SPACER X0910122 PER TI XL 8D 36X12 |
00613994916198 | SPACER X0910107 PER TI LG 8D 30X10 |
00613994916181 | SPACER X0910092 PER TI MD 8D 26X8 |
00613994916174 | SPACER X0910093 PER TI MD 8D 26X10 |
00613994916167 | SPACER X0910094 PER TI MD 8D 26X12 |
00613994916150 | SPACER X0910095 PER TI MD 8D 26X14 |
00613994916143 | SPACER X0910096 PER TI MD 8D 26X16 |
00613994916136 | SPACER X0910097 PER TI MD 8D 26X18 |
00613994916129 | SPACER X0910098 PER TI MD 8D 26X20 |
00613994916112 | SPACER X0910099 PER TI MD 12D 26X8 |
00613994916105 | SPACER X0910100 PER TI MD 12D 26X10 |
00613994916099 | SPACER X0910101 PER TI MD 12D 26X12 |
00613994916082 | SPACER X0910102 PER TI MD 12D 26X14 |
00613994916075 | SPACER X0910103 PER TI MD 12D 26X16 |
00613994916068 | SPACER X0910104 PER TI MD 12D 26X18 |
00613994916051 | SPACER X0910105 PER TI MD 12D 26X20 |
00613994916044 | SPACER X0910106 PER TI LG 8D 30X8 |
00613994916037 | SPACER X1110073 PER TI XXL 8D 38X18 |
00613994916020 | SPACER X1110074 PER TI XXL 8D 38X20 |
00613994916013 | SPACER X1110075 PER TI XXL 12D 38X8 |
00613994916006 | SPACER X1110076 PER TI XXL 12D 38X10 |
00613994915993 | SPACER X1110077 PER TI XXL 12D 38X12 |
00613994915986 | SPACER X1110078 PER TI XXL 12D 38X14 |
00613994915979 | SPACER X1110079 PER TI XXL 12D 38X16 |
00613994915962 | SPACER X1110080 PER TI XXL 12D 38X18 |
00613994915955 | SPACER X1110081 PER TI XXL 12D 38X20 |
00613994915948 | SPACER X1110083 PER TI XXL 15D 38X10 |
00613994915931 | SPACER X1110084 PER TI XXL 15D 38X12 |
00613994915924 | SPACER X1110085 PER TI XXL 15D 38X14 |
00613994915917 | SPACER X1110086 PER TI XXL 15D 38X16 |
00613994915900 | SPACER X1110087 PER TI XXL 15D 38X18 |
00613994915894 | SPACER X1110088 PER TI XXL 15D 38X20 |
00613994915887 | SPACER X1110072 PER TI XXL 8D 38X16 |
00613994915870 | SPACER X0910123 PER TI XL 8D 36X14 |
00613994207043 | SPACER 3494320 PRMTR XLG 8DEG 20MM |
00613994207036 | SPACER 3494318 PRMTR XLG 8DEG 18MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PERIMETER 98488476 not registered Live/Pending |
Tyler Vision LLC 2024-04-08 |
PERIMETER 90182949 not registered Live/Pending |
Song, Dian 2020-09-15 |
PERIMETER 88767043 not registered Live/Pending |
Inteplast Group Corporation 2020-01-21 |
PERIMETER 88189432 not registered Live/Pending |
Ionotronics Corp. 2018-11-11 |
PERIMETER 87324052 5361306 Live/Registered |
ROSEN'S, INC. 2017-02-03 |
PERIMETER 86938932 5492663 Live/Registered |
Milliken & Company 2016-03-14 |
PERIMETER 86926834 5036590 Live/Registered |
Mind Head LLC 2016-03-02 |
PERIMETER 85822820 4813243 Live/Registered |
G-Form, LLC 2013-01-14 |
PERIMETER 85753040 not registered Dead/Abandoned |
Cloud Logix LLC 2012-10-12 |
PERIMETER 85505651 4318256 Live/Registered |
Fast Forward Brands, LLC 2011-12-29 |
PERIMETER 85054256 not registered Dead/Abandoned |
Perimeter Group LLC 2010-06-03 |
PERIMETER 79012773 not registered Dead/Abandoned |
Private Limited Company "K-D LAB" 2005-01-18 |