Primary Device ID | 00613994324092 |
NIH Device Record Key | 289a34c1-d61e-42d2-bd4f-bbf52c439c53 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CD HORIZON® Spinal System |
Version Model Number | X030700208 |
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 |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Outer Diameter | 8 Millimeter |
Length | 25 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994324092 [Primary] |
MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
Moist Heat or Steam Sterilization
[00613994324092]
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 | 2015-08-21 |
00613994953216 | SCR X1010761 5.5 RED SAS TI OGTHN 8.0X95 |
00613994953209 | SCR X1010762 5.5 RED SAS TI OG 8.0X100 |
00613994953193 | SCR X1010750 5.5 RED SAS TI OGTHN 8.0X40 |
00613994953186 | SCR X1010738 5.5 RED SAS TI OGTHN 7.5X65 |
00613994953179 | SCR X1010739 5.5 RED SAS TI OGTHN 7.5X70 |
00613994953162 | SCR X1010740 5.5 RED SAS TI OGTHN 7.5X75 |
00613994953155 | SCR X1010741 5.5 RED SAS TI OGTHN 7.5X80 |
00613994953148 | SCR X1010742 5.5 RED SAS TI OGTHN 7.5X85 |
00613994953131 | SCR X1010743 5.5 RED SAS TI OGTHN 7.5X90 |
00613994953124 | SCR X1010744 5.5 RED SAS TI OGTHN 7.5X95 |
00613994953117 | SCR X1010745 5.5 RED SAS TI OG 7.5X100 |
00613994953100 | SCR X1010746 5.5 RED SAS TI OGTHN 8.0X20 |
00613994953094 | SCR X1010747 5.5 RED SAS TI OGTHN 8.0X25 |
00613994953087 | SCR X1010748 5.5 RED SAS TI OGTHN 8.0X30 |
00613994953070 | SCR X1010749 5.5 RED SAS TI OGTHN 8.0X35 |
00613994951021 | SCREW 54890007585 4.75 RMAS 7.5X85 CC |
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00613994950956 | SCREW 54890008090 4.75 RMAS 8.0X90 CC |
00613994950949 | SCREW 54890008095 4.75 RMAS 8.0X95 CC |
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00613994950826 | SCREW 54890008560 4.75 RMAS 8.5X60 CC |
00613994950819 | SCREW 54890007511 4.75 RMAS 7.5X110 CC |
00613994950802 | SCREW 54890001000 4.75 RMAS 10.0X100 CC |
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00613994950772 | SCREW 54890001080 4.75 RMAS 10.0X80 CC |
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00613994950734 | SCREW 54890001500 4.75 RMAS 10.5X100 CC |
00613994950727 | SCREW 54890001511 4.75 RMAS 10.5X110 CC |
00613994950703 | SCREW 54890001580 4.75 RMAS 10.5X80 CC |
00613994950697 | SCREW 54890001585 4.75 RMAS 10.5X85 CC |
00613994950680 | SCREW 54890001590 4.75 RMAS 10.5X90 CC |
00613994950673 | SCREW 54890001595 4.75 RMAS 10.5X95 CC |
00613994950666 | SCREW 54890004015 4.75 RMAS 4.0X15 CC |
00613994950659 | SCREW 54890004515 4.75 RMAS 4.5X15 CC |
00613994950642 | SCREW 54890005015 4.75 RMAS 5.0X15 CC |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CD HORIZON 75079759 2108361 Live/Registered |
WARSAW ORTHOPEDIC, INC. 1996-03-28 |