Stanmore JTSDF-L-SM

GUDID 05060296236090

JTS Distal Femur Left SM

Stanmore Implants Worldwide Ltd

Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic Uncoated knee femur prosthesis, metallic
Primary Device ID05060296236090
NIH Device Record Keyab0ccad2-a174-4eed-a14f-e8afd7c85c4f
Commercial Distribution StatusIn Commercial Distribution
Brand NameStanmore
Version Model NumberJTSDF-L-SM
Catalog NumberJTSDF-L-SM
Company DUNS494989502
Company NameStanmore Implants Worldwide Ltd
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS105060296236090 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-12-11
Device Publish Date2019-07-18

On-Brand Devices [Stanmore]

05060296233167Bumper Pad XSM
05060296233150Bushes XSM
05060296233136Axle Cap
05060296232825Tibial Rotating Hinge Passive Bearing SM
05060296232818Tibial Rotating Hinge Passive Bearing XSM
05060296232023Circlip
05060296232016Bushes STD
05060296232009Bushes SM
05060296231996Bumper Pad STD
05060296231989Bumper Pad SM
05060296236106JTS Distal Femur Left STD
05060296236090JTS Distal Femur Left SM
05060296236083JTS Distal Femur Left XSM
05060296236076JTS Distal Femur Right STD
05060296236069JTS Distal Femur Right SM
05060296236052JTS Distal Femur Right XSM
05060296232832Tibial Rotationg Hinge Passive Bearing STD
05060296235970Tibial Rotating Hinge Metal Cased Bearing XSM
05060296232849Tibial Rotating Hinge Poly Cased Bearing XSM
05060296232061Tibial Rotating Hinge Poly Cased Bearing STD
05060296232054Tibial Rotating Hinge Poly Cased Bearing SM
05060296232047Tibial Rotating Hinge Metal Cased Bearing STD
05060296232030Tibial Rotating Hinge Metal Cased Bearing SM
05060296230340Tibial Plateau Plate STD 20mm
05060296230333Tibial Plateau Plate STD 15mm
05060296230326Tibial Plateau Plate STD 10mm
05060296230319Tibial Plateau Plate STD 5mm
05060296230302Tibial Plateau Plate SM 20mm
05060296230296Tibial Plateau Plate SM 15mm
05060296230289Tibial Plateau Plate SM 10mm
05060296230272Tibial Plateau Plate SM 5mm

Trademark Results [Stanmore]

Mark Image

Registration | Serial
Company
Trademark
Application Date
STANMORE
STANMORE
79147306 4718582 Live/Registered
Marshall Amplification Plc
2013-12-05

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.