MATRIXWAVE 0450382501

GUDID H98004503825010

MATRIXWAVE MMF TI 1.85MM SCREW SELF-DRILLING/8MM LENGTH

SYNTHES (U.S.A.) LP

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable
Primary Device IDH98004503825010
NIH Device Record Key603f11d7-9eac-47ea-adeb-1ece6059fe99
Commercial Distribution StatusIn Commercial Distribution
Brand NameMATRIXWAVE
Version Model Number04.503.825.01
Catalog Number0450382501
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110887587069487 [Primary]
HIBCCH98004503825010 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H98004503825010]

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[H98004503825010]

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[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


[H98004503825010]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-14

On-Brand Devices [MATRIXWAVE]

H98004503825050MATRIXWAVE MMF TI 1.85MM SCREW SELF-DRILLING/8MM LENGTH
H98004503824050MATRIXWAVE MMF TI 1.85MM SCREW SELF-DRILLING/6MM LENGTH
07612334093486MATRIXWAVE MMF APPLICATION INSTRUMENT
H98004503825010MATRIXWAVE MMF TI 1.85MM SCREW SELF-DRILLING/8MM LENGTH
H98004503824010MATRIXWAVE MMF TI 1.85MM SCREW SELF-DRILLING/6MM LENGTH
H980045038210MATRIXWAVE MMF TI PLATE 10 HOLES/TALL
H980045038200MATRIXWAVE MMF TI PLATE 10 HOLES/SHORT
07612334094780MATRIXWAVE MMF SYSTEM INSERT TRAY ID TAG F/PLATES
07612334094773MATRIXWAVE MMF INSERT TRAY ID TAG F/1.85MM LOCKING SCREWS
07612334094766MATRIXWAVE MMF SYSTEM INSERT TRAY F/1.85MM LOCKING SCREWS
07612334094759MATRIXWAVE MMF SYSTEM IMPLANT MODULE ID TAG
07612334093547MATRIXWAVE MMF SYSTEM INSTRUMENT MODULE ID TAG
07612334093530MATRIXWAVE MMF SYSTEM MODULE LID
07612334093523MATRIXWAVE MMF SYSTEM IMPLANT MODULE BASE
07612334093516MATRIXWAVE MMF SYSTEM INSTRUMENT MODULE BASE

Trademark Results [MATRIXWAVE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MATRIXWAVE
MATRIXWAVE
86318318 4823301 Live/Registered
DePuy Synthes, Inc.
2014-06-24

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