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FDA 510(k)

AART CHIN IMPLANT

K-Number: K021417 · 2002-07-02

ApplicantAesthetic and Reconstructive Technologies, Inc.
Decision Date2002-07-02
Product CodeFWP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AART CHIN IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetic and Reconstructive Technologies, Inc.. It received FDA 510(k) clearance on 2002-07-02 under 510(k) number K021417. The device is classified under product code FWP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AART CHIN IMPLANT?

AART CHIN IMPLANT is a medical device that received FDA 510(k) clearance on 2002-07-02. The listed applicant is Aesthetic and Reconstructive Technologies, Inc.. The 510(k) number is K021417.

When did AART CHIN IMPLANT receive FDA 510(k) clearance?

AART CHIN IMPLANT received FDA 510(k) clearance on 2002-07-02, under 510(k) number K021417.

Who is the listed applicant for AART CHIN IMPLANT?

The FDA 510(k) record lists Aesthetic and Reconstructive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AART CHIN IMPLANT?

The FDA product code for AART CHIN IMPLANT is FWP.

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Other records listing Aesthetic and Reconstructive Technologies, 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.

K023678DIMISIL SCAR GELK022306AART SILICONE TUBINGK022511AART CALF IMPLANTK022223AART SILICONE SHEETINGK021839AART GLUTEAL IMPLANTK021820AART SILICONE CARVING BLOCK

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Related Devices (Code: FWP)

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.

K254233MEDPOR Customized Implant KitStryker Leibinger GmbH & Co KGK232593FITme Customized Silicone ImplantKeosan Trading Co.K200610Customized Contour ImplantImplantech Associates, Inc.K191130Customized Contour ImplantImplantech Associates, Inc.K191916Stryker CMF MEDPOR Priority Customized Implant KitStryker Leibinger GmbH & Co KGK153508Stryker CMF MEDPOR Customized ImplantStryker

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.

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