UCSS® Screw Set

GUDID 00673978067872

BONE SCREW 873-046 4.0 CANN CORT L 46MM

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00673978067872
NIH Device Record Keyc2ad9793-3258-4a4f-9d5f-312d2f11ad46
Commercial Distribution StatusIn Commercial Distribution
Brand NameUCSS® Screw Set
Version Model Number873-046
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Outer Diameter4 Millimeter
Outer Diameter4 Millimeter
Outer Diameter4 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter
Length46 Millimeter
Outer Diameter4 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978067872 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MRWSYSTEM, FACET SCREW SPINAL DEVICE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


[00673978067872]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-18

On-Brand Devices [UCSS® Screw Set]

00613994264237SCREW X10043510 TI 3.5X10MM THRPST
00673978067971BONE SCREW 873-150 4.0 CAN CORT LAG L 50
00673978067964BONE SCREW 873-148 4.0 CAN CORT LAG L 48
00673978067957BONE SCREW 873-146 4.0 CAN CORT LAG L 46
00673978067940BONE SCREW 873-144 4.0 CAN CORT LAG L 44
00673978067933BONE SCREW 873-142 4.0 CAN CORT LAG L 42
00673978067926BONE SCREW 873-140 4.0 CAN CORT LAG L 40
00673978067919BONE SCREW 873-138 4.0 CAN CORT LAG L 38
00673978067902BONE SCREW 873-136 4.0 CAN CORT LAG L 36
00673978067896BONE SCREW 873-050 4.0 CANN CORT L 50MM
00673978067889BONE SCREW 873-048 4.0 CANN CORT L 48MM
00673978067872BONE SCREW 873-046 4.0 CANN CORT L 46MM
00673978067865BONE SCREW 873-044 4.0 CANN CORT L 44MM
00673978067858BONE SCREW 873-042 4.0 CANN CORT L 42MM
00673978067841BONE SCREW 873-040 4.0 CANN CORT L 40MM
00673978067834BONE SCREW 873-038 4.0 CANN CORT L 38MM
00673978067827BONE SCREW 873-036 4.0 CANN CORT L 36MM
00673978067810BONE SCREW 873-034 4.0 CANN CORT L 34MM
00673978067803BONE SCREW 873-032 4.0 CANN CORT L 32MM
00673978067797BONE SCREW 873-030 4.0 CANN CORT L 30MM
00721902613371UCS DBLTHDSCR-TI-CANN-4.0X40
007219023198154.0 CORTICAL BONE SCREW 60MM
007219023197924.0 CORTICAL BONE SCREW 58MM
007219023197854.0 CORTICAL BONE SCREW 56MM
007219023197784.0 CORTICAL BONE SCREW 54MM
007219023197474.0 CORTICAL BONE SCREW 52MM
007219023197304.0 CORTICAL BONE SCREW 50MM
007219023197094.0 CORTICAL BONE SCREW 48MM
007219023196934.0 CORTICAL BONE SCREW 46MM
007219023196864.0 CORTICAL BONE SCREW 44MM
007219023196794.0 CORTICAL BONE SCREW 42MM
007219023196554.0 CORTICAL BONE SCREW 40MM
007219023196174.0 CORTICAL BONE SCREW 38MM
007219023195324.0 CORTICAL BONE SCREW 34MM
007219023195184.0 CORTICAL BONE SCREW 30MM
007219023194954.0 CORTICAL BONE SCREW 26MM
00673978067759CASE 873-012 UCSS INSTRUMENT MODULE

Trademark Results [UCSS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
UCSS
UCSS
78357555 2974437 Live/Registered
WARSAW ORTHOPEDIC, INC.
2004-01-26
UCSS
UCSS
75557936 not registered Dead/Abandoned
SDGI Holdings, Inc.
1998-09-23

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