TrueLok 99-56-13650

GUDID 18053340349611

TL+ FOOTPLATE 180MM STERILE

ORTHOFIX SRL

External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use, sterile External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use
Primary Device ID18053340349611
NIH Device Record Keyac788538-3bc2-423c-8339-07df1497d327
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrueLok
Version Model Number1
Catalog Number99-56-13650
Company DUNS438793622
Company NameORTHOFIX SRL
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it
Phone0456719000
Emailinfo@orthofix.it

Device Dimensions

Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter
Lumen/Inner Diameter170 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS118053340349611 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-25
Device Publish Date2021-06-17

On-Brand Devices [TrueLok]

18053340349529TL+ FOOTPLATE 100MM STERILE
18053340349512TL PLUS FIVE EIGHTHS RING 200MM STERILE
18053340349505TL PLUS FIVE EIGHTHS RING 180MM STERILE
18053340349499TL PLUS FIVE EIGHTHS RING 170MM STERILE
18053340349482TL PLUS FIVE EIGHTHS RING 160MM STERILE
18053340349475TL PLUS FIVE EIGHTHS RING 150MM STERILE
18053340349468TL PLUS FIVE EIGHTHS RING 140MM STERILE
18053340349451TL PLUS FIVE EIGHTHS RING 130MM STERILE
18053340349444TL PLUS FIVE EIGHTHS RING 120MM STERILE
18053340349437TL PLUS FIVE EIGHTHS RING 100MM STERILE
18053340349420TL PLUS HALF RING 240MM STERILE
18053340349413TL PLUS HALF RING 220MM STERILE
18053340349406TL PLUS HALF RING 200MM STERILE
18053340349390TL PLUS HALF RING 180MM STERILE
18053340349383TL PLUS HALF RING 170MM STERILE
18053340349376TL PLUS HALF RING 160MM STERILE
18053340349369TL PLUS HALF RING 150MM STERILE
18053340349352TL PLUS HALF RING 140MM STERILE
18053340349345TL PLUS HALF RING 130MM STERILE
18053340349338TL PLUS HALF RING 120MM STERILE
18053340349321TL PLUS HALF RING 100MM STERILE
18053340349314TL PLUS HALF RING 80MM STERILE
18053340349307TL PLUS FULL RING, 240MM STERILE
18053340349291TL PLUS FULL RING, 220MM STERILE
18053340349284TL PLUS FULL RING, 200MM STERILE
18053340349277TL PLUS FULL RING, 180MM STERILE
18053340349260TL PLUS FULL RING, 170MM STERILE
18053340349253TL PLUS FULL RING, 160MM STERILE
18053340349246TL PLUS FULL RING, 150MM STERILE
18053340349239TL PLUS FULL RING, 140MM STERILE
18053340349222TL PLUS FULL RING, 130MM STERILE
18053340349215TL PLUS FULL RING, 120MM STERILE
18053340349208TL PLUS FULL RING 100MM STERILE
18053340349192TL PLUS FULL RING 80MM STERILE
18053340349673TL TRAUMA STRUT STERILE
18053340349666TRUE LOK TRAUMA U-SUPPORT, 180MM STERILE
18053340349659TRUE LOK TRAUMA U-SUPPORT, 160MM STERILE
18053340349642200 MM DOUBLE ROW FOOT PLATE STERILE
18053340349635TL+ FOOTPLATE 200MM STERILE
18053340349628180 MM DOUBLE ROW FOOT PLATE STERILE
18053340349611TL+ FOOTPLATE 180MM STERILE
18053340349604TL+ FOOTPLATE 170MM STERILE
18053340349598160 MM DOUBLE ROW FOOT PLATE STERILE
18053340349581TL+ FOOTPLATE 160MM STERILE
18053340349574150 MM DOUBLE ROW FOOT PLATE STERILE
18053340349567TL PLUS FOOTPLATE 150MM STERILE
18053340349550TL+ FOOTPLATE 140MM STERILE
18053340349543TL+ FOOTPLATE 130MM STERILE
18053340349536TL PLUS FOOTPLATE 120MM STERILE
18052469472880TRUELOK FOOT LEG ALIGNMENT SUPPORT PACK OF 3 STERILE

Trademark Results [TrueLok]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRUELOK
TRUELOK
97044556 not registered Live/Pending
Texas Scottish Rite Hospital for Crippled Children
2021-09-24
TRUELOK
TRUELOK
85232653 4028273 Live/Registered
CMAX-2000, INC.
2011-02-02

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