WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY

Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer

DOW CORNING WRIGHT

The following data is part of a premarket notification filed by Dow Corning Wright with the FDA for Whiteside Ortholoc Ii Rev Post Stab Total Knee Sy.

Pre-market Notification Details

Device IDK871776
510k NumberK871776
Device Name:WHITESIDE ORTHOLOC II REV POST STAB TOTAL KNEE SY
ClassificationProsthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Applicant DOW CORNING WRIGHT P.O. BOX 100 Arlington,  TN  38002
ContactLipscomb, Phd
CorrespondentLipscomb, Phd
DOW CORNING WRIGHT P.O. BOX 100 Arlington,  TN  38002
Product CodeJWH  
CFR Regulation Number888.3560 [🔎]
DecisionSubstantially Equivalent For Some Indications (SN)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-05-06
Decision Date1987-08-03

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