KT2000 KNEE LIGAMENT ARTHROMETER

Arthrometer

MEDMETRIC CORP.

The following data is part of a premarket notification filed by Medmetric Corp. with the FDA for Kt2000 Knee Ligament Arthrometer.

Pre-market Notification Details

Device IDK942059
510k NumberK942059
Device Name:KT2000 KNEE LIGAMENT ARTHROMETER
ClassificationArthrometer
Applicant MEDMETRIC CORP. 7542 TRADE ST. San Diego,  CA  92121 -2412
ContactK.r. Watkins
CorrespondentK.r. Watkins
MEDMETRIC CORP. 7542 TRADE ST. San Diego,  CA  92121 -2412
Product CodeLYH  
CFR Regulation Number890.1615 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1994-04-29
Decision Date1994-09-20

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