Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Silhouette Featherlift

K-Number: K171005 · 2017-05-03

Decision Date2017-05-03
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Silhouette Featherlift is the device name listed in this FDA 510(k) record. The listed applicant is Silhouette Lift, Inc.. It received FDA 510(k) clearance on 2017-05-03 under 510(k) 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. The listed applicant is Silhouette Lift, Inc.. The 510(k) number is K171005.

When did Silhouette Featherlift receive FDA 510(k) clearance?

Silhouette Featherlift received FDA 510(k) clearance on 2017-05-03, under 510(k) number K171005.

Who is the listed applicant for Silhouette Featherlift?

The FDA 510(k) record lists Silhouette Lift, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Silhouette Featherlift?

The FDA product code for Silhouette Featherlift is GAW.

Other records listing Silhouette Lift, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GAW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.