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FDA 510(k)

Silhouette Featherlift / Silhouette Lift

K-Number: K191299 · 2019-06-14

ApplicantSilhouette Lift, Inc.
Decision Date2019-06-14
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Silhouette Featherlift / Silhouette Lift 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 2019-06-14 under 510(k) number K191299. 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 Lift?

Silhouette Featherlift / Silhouette Lift is a medical device that received FDA 510(k) clearance on 2019-06-14. The listed applicant is Silhouette Lift, Inc.. The 510(k) number is K191299.

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

Silhouette Featherlift / Silhouette Lift received FDA 510(k) clearance on 2019-06-14, under 510(k) number K191299.

Who is the listed applicant for Silhouette Featherlift / Silhouette Lift?

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 / Silhouette Lift?

The FDA product code for Silhouette Featherlift / Silhouette Lift 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.

K200140Silhouette InstaliftK163676Silhouette InstaLiftK171005Silhouette Featherlift

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.

K253572STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™ Spiral PRONOVA™ Bidirectional Knotless Tissue Control DeviceETHICON, Inc.K233355Cypris eXact Suturing SystemCypris MedicalK230746Non absorbable Surgical Polypropylene SutureShandong Haidike Medical Products Co., Ltd.K221280VessealLydus Medical , Ltd.K211178DURAMESH Mesh SutureMsiK192953APTOS Threads – Polypropylene Surgical SuturesAptos, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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