CATALYST® Reusable Instruments

GUDID 00885074058153

INSTRUMENT 3289810 OBL PREC SPREADR 10MM

MEDTRONIC SOFAMOR DANEK, INC.

Orthopaedic prosthesis implantation instrument, reusable
Primary Device ID00885074058153
NIH Device Record Key59966af0-c808-4e0c-9735-53a332d176f6
Commercial Distribution StatusIn Commercial Distribution
Brand NameCATALYST® Reusable Instruments
Version Model Number3289810
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 Usefalse
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

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100885074058153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


[00885074058153]

Moist Heat or Steam Sterilization


Device Entry Metadata

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

Devices Manufactured by MEDTRONIC SOFAMOR DANEK, INC.

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00763000875282 - SHILLA™ Growth Guidance System2025-10-06 SCREW 7675430 5.5 SHILLA MAS CANN 4.5X30
00763000884956 - n/a2025-10-06 LOCK SCREW DRIVER 7080930 TRI-FLAT
00885074240695 - n/a2025-09-30 ACCESSORIES 3299003 GRAFT TAMP
00199150026029 - Medtronic Reusable Instruments2025-09-29 COMPRESSOR X0525001 RACK AND PINION
00763000684044 - Medtronic Reusable Instruments2025-09-29 INSTRUMENT 950-146 RULER
00763000856700 - VERTE-STACK® Spinal System2025-09-29 STRUT 6242064 ANATOMIC 16X14X24MM
00763000879563 - ENDOSKELETON® TCS2025-09-29 HANDLE 5210-1016 TCS RATCHETING HANDLE

Trademark Results [CATALYST]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CATALYST
CATALYST
98784854 not registered Live/Pending
Partnership Leaders, Inc.
2024-10-03
CATALYST
CATALYST
98784846 not registered Live/Pending
Partnership Leaders, Inc.
2024-10-03
CATALYST
CATALYST
98700380 not registered Live/Pending
Siragusa, Dominic
2024-08-15
CATALYST
CATALYST
98700068 not registered Live/Pending
FCA US LLC
2024-08-15
CATALYST
CATALYST
98677986 not registered Live/Pending
Xanadu Quantum Technologies Inc.
2024-08-01
CATALYST
CATALYST
98662690 not registered Live/Pending
OLDCASTLE APG, INC.
2024-07-23
CATALYST
CATALYST
98606318 not registered Live/Pending
John Wiley & Sons, Inc.
2024-06-18
CATALYST
CATALYST
98565447 not registered Live/Pending
Blue Lion Consulting LLC
2024-05-23
CATALYST
CATALYST
98508136 not registered Live/Pending
DRB Systems, LLC
2024-04-18
CATALYST
CATALYST
98508129 not registered Live/Pending
DRB Systems, LLC
2024-04-18
CATALYST
CATALYST
98433801 not registered Live/Pending
John Wiley & Sons, Inc.
2024-03-05
CATALYST
CATALYST
98415936 not registered Live/Pending
Sustained Quality LLC
2024-02-22

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