CURETTE

Curette, Ear

TREACE MEDICAL, INC.

The following data is part of a premarket notification filed by Treace Medical, Inc. with the FDA for Curette.

Pre-market Notification Details

Device IDK841354
510k NumberK841354
Device Name:CURETTE
ClassificationCurette, Ear
Applicant TREACE MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJYG  
CFR Regulation Number874.4420 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-04-02
Decision Date1984-07-06

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