Silhouette Featherlift

Suture, Nonabsorbable, Synthetic, Polypropylene

Silhouette Lift Inc.

The following data is part of a premarket notification filed by Silhouette Lift Inc. with the FDA for Silhouette Featherlift.

Pre-market Notification Details

Device IDK171005
510k NumberK171005
Device Name:Silhouette Featherlift
ClassificationSuture, Nonabsorbable, Synthetic, Polypropylene
Applicant Silhouette Lift Inc. 1 Technology Drive F211 Irvine,  CA  92618
ContactAnthony Dibernardo
CorrespondentAnthony Dibernardo
Silhouette Lift Inc. 1 Technology Drive F211 Irvine,  CA  92618
Product CodeGAW  
CFR Regulation Number878.5010 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-04-04
Decision Date2017-05-03
Summary:summary

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