LM BONE ANCHOR

Fastener, Fixation, Nondegradable, Soft Tissue

LI MEDICAL TECHNOLOGIES, INC.

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

Pre-market Notification Details

Device IDK960439
510k NumberK960439
Device Name:LM BONE ANCHOR
ClassificationFastener, Fixation, Nondegradable, Soft Tissue
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 CodeMBI  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-01-31
Decision Date1996-04-18
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20845854040321 K960439 000
20845854040291 K960439 000
10845854037096 K960439 000
10845854015971 K960439 000
20845854015657 K960439 000

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