MOORE TYPE ENDO PROSTHESIS

Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented

LIMA INTL. CORP.

The following data is part of a premarket notification filed by Lima Intl. Corp. with the FDA for Moore Type Endo Prosthesis.

Pre-market Notification Details

Device IDK900051
510k NumberK900051
Device Name:MOORE TYPE ENDO PROSTHESIS
ClassificationProsthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented
Applicant LIMA INTL. CORP. 392 WAMPANOAG TRAIL E Providence,  RI  02915
ContactPollonio-lister
CorrespondentPollonio-lister
LIMA INTL. CORP. 392 WAMPANOAG TRAIL E Providence,  RI  02915
Product CodeKWY  
CFR Regulation Number888.3390 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-01-03
Decision Date1990-10-03

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