NEXA COMPRESSION SCREW

Screw, Fixation, Bone

NEXA ORTHOPEDICS, INC.

The following data is part of a premarket notification filed by Nexa Orthopedics, Inc. with the FDA for Nexa Compression Screw.

Pre-market Notification Details

Device IDK060071
510k NumberK060071
Device Name:NEXA COMPRESSION SCREW
ClassificationScrew, Fixation, Bone
Applicant NEXA ORTHOPEDICS, INC. 10675 SORRENTO VALLEY ROAD SUITE 100 San Diego,  CA  92121
ContactLouise M Focht
CorrespondentLouise M Focht
NEXA ORTHOPEDICS, INC. 10675 SORRENTO VALLEY ROAD SUITE 100 San Diego,  CA  92121
Product CodeHWC  
CFR Regulation Number888.3040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-01-09
Decision Date2006-01-26
Summary:summary

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