Instrument

Primary DI
05060296236007
Brand
Instrument
Company
Stanmore Implants Worldwide Ltd
Model
MLE3
Catalog number
JTS-DRIVE-UNIT
Device description
JTS Drive Unit Set
Published
2019-07-18
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/PolymerOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K092138000
K133152000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K092138000JTS EXTENDEABLE IMPLANTStanmore Implants Worldwide , Ltd.2011-03-22KRO
K133152000JTS EXTENDIBLE DISTAL FEMORAL IMPLANTStanmore Implants Worldwide , Ltd.2014-01-22KRO

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05060296236007PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05060296236007050602962360075060296236007

GMDN Terms#

Term, Definition table
TermDefinition
Extremity MRI system, resistive magnetA diagnostic magnetic resonance imaging (MRI) system employing resistive magnet technology specifically designed to image only the head and neck or limbs. An extremity imaging system is typically closed bore design with cylindrical or rectangular bore openings but can be "open" bore design. This device includes MRI systems with conventional extremity capabilities, conventional systems capable of performing spectroscopy or other real-time imaging procedures necessary for interventional and therapeutic MRI applications, and dedicated magnetic resonance (MR) spectroscopy systems.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
494989502
Device count
1
Serial number
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05060296233839InstrumentimgenimpIMGENIMP2019-07-18
05060296233853Instrumentimpbimp/StdIMPBIMP-STD2019-07-18
05060296233877Instrumentimpbimp/SmIMPBIMP-SM2019-07-18
05060296236182Instrumentimpbimp/ExSmIMPBIMP-EXSM2019-07-18
05060296233693InstrumentimcirprIMCIRPR2019-07-18
05060296236397InstrumentibnpinPINS2019-07-18
05060296233709InstrumentimtrfhIMTRFH2019-07-18
05060296233761Instrumentimtrrhm/StdIMTRRHM-STD2019-07-18
05060296233778Instrumentimtrrhm/SmIMTRRHM-SM2019-07-18
05060296233846Instrumentimtrrhp/SmIMTRRHP-SM2019-07-18
05060296233860Instrumentimtrrhp/StdIMTRRHP-STD2019-07-18
05060296236151Instrumentimtrrhm/ExSmIMTRRHM-EXSM2019-07-18
05060296236175Instrumentimtrrhp/ExSmIMTRRHP-EXSM2019-07-18
05060296236304Instrumentimtrp/ExSmIMTRP-EXSM2019-07-18
05060296236311Instrumentimtrp/SmIMTRP-SM2019-07-18
05060296236328Instrumentimtrp/StdIMTRP-STD2019-07-18
05060296230272Stanmoremktp/Sm5MKTP-SM52019-07-18
05060296230289Stanmoremktp/Sm10MKTP-SM102019-07-18
05060296230296Stanmoremktp/Sm15MKTP-SM152019-07-18
05060296230302Stanmoremktp/Sm20MKTP-SM202019-07-18

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Primary DI, Brand, Company table
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