Silhouette Featherlift
K-Number: K171005 · 2017-05-03
ApplicantSilhouette Lift, Inc.
Decision Date2017-05-03
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Silhouette Featherlift is a medical device manufactured by Silhouette Lift, Inc.. It received FDA 510(k) clearance on 2017-05-03 under approval number K171005. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Silhouette Featherlift?
Silhouette Featherlift is a medical device that received FDA 510(k) clearance on 2017-05-03. It is manufactured by Silhouette Lift, Inc.. The 510(k) number is K171005.
When was Silhouette Featherlift approved by the FDA?
Silhouette Featherlift received FDA 510(k) clearance on 2017-05-03, under approval number K171005.
What company makes Silhouette Featherlift?
Silhouette Featherlift is manufactured by Silhouette Lift, Inc..
What is the FDA product code for Silhouette Featherlift?
The FDA product code for Silhouette Featherlift is GAW.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.