XPE Patellar, On set, 3 pegs 2403-3220

GUDID 04712771485271

XPE Patellar, On set, 3 pegs, Small, ψ 29 mm

UNITED ORTHOPEDIC CORP.

Cruciate-retaining total knee prosthesis
Primary Device ID04712771485271
NIH Device Record Key765e76ba-5432-47d1-8ac0-983281fadb10
Commercial Distribution StatusIn Commercial Distribution
Brand NameXPE Patellar, On set, 3 pegs
Version Model Number2403-3220
Catalog Number2403-3220
Company DUNS656700556
Company NameUNITED ORTHOPEDIC CORP.
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+886229294567
Emailservice@uoc.com.tw

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104712771485271 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-13
Device Publish Date2015-10-24

On-Brand Devices [XPE Patellar, On set, 3 pegs]

04712771485325XPE Patellar, On set, 3 pegs, E-Larger, ψ 44 mm
04712771485318XPE Patellar, On set, 3 pegs, XX-Larger, ψ 41 mm
04712771485301XPE Patellar, On set, 3 pegs, X-Larger, ψ 38 mm
04712771485295XPE Patellar, On set, 3 pegs, Larger, ψ 35 mm
04712771485288XPE Patellar, On set, 3 pegs, Medium,ψ 32 mm
04712771485271XPE Patellar, On set, 3 pegs, Small, ψ 29 mm
04712771485264XPE Patellar, On set, 3 pegs, X-Small, ψ 26 mm

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