KMBClass IIImplant

Prosthesis, Knee, Non-constrained (metal-carbon Reinforced Polyethylene) Cemented

Orthopedic · 21 CFR 888.3490

MDR events8All time

Recalls0All time

Registered firms0Currently listed

510(k) clearances0All time

Recent MDR events

8 adverse event reports on file

E.MOTION PS MENISCAL COMPONENT F6L 10MMJul 9, 2025
InjuryAesculap Ag9610612-2025-00138
STRYKER SCORPIO NRGFeb 5, 2013
MalfunctionStryker2948708
ROBERT BRIGHAM UNI-CONDYLAR KNEE - REINFORCED TIBIAL PLATEAUJul 18, 1994
MalfunctionJohnson & Johnson Roducts, Inc. - Orthopaedics8276
ROBERT BRIGHAM UNI-CONDYLAR KNEE - REINFORCED TIBIAL PLATEAUApr 26, 1994
MalfunctionJohnson & Johnson Products, Inc. - Orthopaedics Div.7732
KINEMATIC KNEEJan 14, 1994
InjuryHowmedica, Inc.33446-1993-00060
UNKNOWNAug 16, 1993
InjuryUnknown6330
PCA LG. 7MM TIBIAL COMPONENTMar 1, 1993
InjuryHowmedica, Inc33274-1993-00007
WHITESIDE I TOTAL KNEE IMPLANTJul 31, 1992
MalfunctionDow-corning3470

Event type breakdown

Injury4

Malfunction4

Most-reported manufacturers

Aesculap Ag1 Dow-corning1 Howmedica, Inc1 Howmedica, Inc.1 Johnson & Johnson Products, Inc. - Orthopaedics Div.1 Johnson & Johnson Roducts, Inc. - Orthopaedics1 Stryker1 Unknown1

Recalls

0 recall events for this product code

No recalls on file for this product code.

Registered firms

0 firms currently registered for this product code

No registered firms found for this product code.

510(k) clearances

0 clearances for this product code

No 510(k) clearances on file for this product code.