DEPUY ACE SPIDER PLATE

Plate, Fixation, Bone

DEPUY ACE MEDICAL CO.

The following data is part of a premarket notification filed by Depuy Ace Medical Co. with the FDA for Depuy Ace Spider Plate.

Pre-market Notification Details

Device IDK990392
510k NumberK990392
Device Name:DEPUY ACE SPIDER PLATE
ClassificationPlate, Fixation, Bone
Applicant DEPUY ACE MEDICAL CO. 2260 EAST EL SEGUNDO BLVD. El Segundo,  CA  90245
ContactKathleen Dragovich
CorrespondentKathleen Dragovich
DEPUY ACE MEDICAL CO. 2260 EAST EL SEGUNDO BLVD. El Segundo,  CA  90245
Product CodeHRS  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-02-09
Decision Date1999-03-23
Summary:summary

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