Femoral Component 51125PF

GUDID EPIS51125PF0

Episurf Operations AB

Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis Patellofemoral joint prosthesis
Primary Device IDEPIS51125PF0
NIH Device Record Key51f5cbac-b401-47f3-8b11-43adae81ec83
Commercial Distribution StatusIn Commercial Distribution
Brand NameFemoral Component
Version Model Number2xD25
Catalog Number51125PF
Company DUNS352393402
Company NameEpisurf Operations AB
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEPIS51125PF0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRRProsthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-01
Device Publish Date2023-07-24

On-Brand Devices [Femoral Component]

EPIS51125PF02xD25
EPIS51120PF02xD20
EPIS51117PF02xD17
EPIS31129PF0D29
EPIS31125PF0D25
EPIS31120PF0D20

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