LMT BONE ANCHOR

Screw, Fixation, Bone

LI MEDICAL TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Li Medical Technologies, Inc. with the FDA for Lmt Bone Anchor.

Pre-market Notification Details

Device IDK951472
510k NumberK951472
Device Name:LMT BONE ANCHOR
ClassificationScrew, Fixation, Bone
Applicant LI MEDICAL TECHNOLOGIES, INC. 4 ARMSTRONG RD. Shelton,  CT  06484
ContactRhodemann Li
CorrespondentRhodemann Li
LI MEDICAL TECHNOLOGIES, INC. 4 ARMSTRONG RD. Shelton,  CT  06484
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-03-30
Decision Date1995-07-03

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