OSTEO TIBIA NAIL

Rod, Fixation, Intramedullary And Accessories

OSTEO AG

The following data is part of a premarket notification filed by Osteo Ag with the FDA for Osteo Tibia Nail.

Pre-market Notification Details

Device IDK922196
510k NumberK922196
Device Name:OSTEO TIBIA NAIL
ClassificationRod, Fixation, Intramedullary And Accessories
Applicant OSTEO AG 208 WILSON BRIDGE RD. Greenwood,  SC  29646
ContactBryson, Jr.
CorrespondentBryson, Jr.
OSTEO AG 208 WILSON BRIDGE RD. Greenwood,  SC  29646
Product CodeHSB  
CFR Regulation Number888.3020 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-05-11
Decision Date1992-07-23

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