FDA.reportPublic FDA data

TRUE/LOK MONOLATERAL/BILATERAL FIXATOR

Primary DI
18053340349581
Brand
TRUE/LOK MONOLATERAL/BILATERAL FIXATOR
Company
ORTHOFIX SRL
Model
1
Catalog number
99-56-13630
Device description
TL+ FOOTPLATE 160MM STERILE
Published
2021-06-17
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LXTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal CompositeOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K941048000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K941048000TRUE/LOK MONOLATERAL/BILATERAL FIXATORApplied Osteo Systems, Inc.1994-10-03LXT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
18053340349581PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1805334034958118053340349581

GMDN Terms#

Term, Definition table
TermDefinition
External orthopaedic fixation system, single-use, sterileAn assembly of sterile devices designed to stabilize fractured bones of the lower limbs to promote treatment and healing. It typically consists of an external plastic and/or metallic fixator (a framework) and other external and/or implantable components such as clamps, rods, rings, pins, bolts, and nuts, as well as some reusable instrumentation (e.g., wrenches, depth gauge, tensioner). It is used mainly to help the healing of long bones such as the femur and tibia, as well as fractures of the foot and ankle, joint fusions, and limb lengthening. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Lumen/Inner Diameter160Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
0456719000info@orthofix.it
+0390456719000info@orthofix.it

Regulatory Flags#

DUNS number
438793622
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
18059015375831OrthoNext™ Platform System Software2.1ORTHONEXTSW2.12025-01-31
18059015375848OrthoNext™ Platform System Software1.1TLHEXMODULESW1.12025-01-31
18052469476444OrthoNext™ Platform System Software1.0TLHEXMODULESW2023-03-31
18052469476451OrthoNext™ Platform System Software1.0MYHEXPLANSW2023-03-31
18053340345675OrthoNext™ Platform System Software2.0ORTHONEXTSW2023-03-31
18053340345682OrthoNext™ Platform System Software1.1JPSMODULESW2023-03-31
18032568033229Surgical Instruments1136202026-07-23
18032568033236Surgical Instruments1136212026-07-23
18032568036008WRIST FIXATION SYSTEMS1360082026-07-23
18059015376838Fitbone Transport and Lengthening System199-600038172026-07-23
18059015376845Fitbone Transport and Lengthening System199-600038182026-07-23
18059015376852Fitbone Transport and Lengthening System199-600038192026-07-23
18059015376869Fitbone Transport and Lengthening System199-600038202026-07-23
18059015376876Fitbone Transport and Lengthening System199-600038212026-07-23
18059015376883Fitbone Transport and Lengthening System199-600038222026-07-23
18059015376890Fitbone Transport and Lengthening System199-600038232026-07-23
18059015376906Fitbone Transport and Lengthening System199-600038242026-07-23
18059015376913Fitbone Transport and Lengthening System199-600038252026-07-23
18059015376920Fitbone Transport and Lengthening System199-600038262026-07-23
18059015376937Fitbone Transport and Lengthening System199-600038272026-07-23

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00887868549236MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549243MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549250MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549267MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549274MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549281MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549298MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549304MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549311MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549328MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549335MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549342MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549359MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549366MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549373MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868549380MULTI-DIRECTIONAL SCREWBiomet Orthopedics, LLCLXT2022-11-14
00887868544699SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544705SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544712SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544729SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544736SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544743SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544750SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544767SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544774SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544781SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544798SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544804SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544811SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07
00887868544828SMOOTH PEGBiomet Orthopedics, LLCLXT2022-09-07