TAPERLOC COMPLETE SIZE 4MM AND XR 123

Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented

BIOMET MANUFACTURING CORP.

The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Taperloc Complete Size 4mm And Xr 123.

Pre-market Notification Details

Device IDK120030
510k NumberK120030
Device Name:TAPERLOC COMPLETE SIZE 4MM AND XR 123
ClassificationProsthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented
Applicant BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw,  IN  46581 -0587
ContactBecky Earl
CorrespondentBecky Earl
BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw,  IN  46581 -0587
Product CodeLPH  
Subsequent Product CodeJDI
Subsequent Product CodeKWL
Subsequent Product CodeKWY
Subsequent Product CodeKWZ
Subsequent Product CodeLZO
Subsequent Product CodeMEH
Subsequent Product CodeOQG
CFR Regulation Number888.3358 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2012-01-04
Decision Date2012-08-17
Summary:summary

NIH GUDID Devices

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