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AART PECTORALIS IMPLANT — Aesthetic and Reconstructive Technologies, Inc. (510(k) K021337)

AART PECTORALIS IMPLANT — Aesthetic and Reconstructive Technologies, Inc. (510(k) K021337) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AART PECTORALIS IMPLANT; Applicant: Aesthetic and Reconstructive Technologies, Inc.; Clearance track: 510(k).

Device nameAART PECTORALIS IMPLANT
ApplicantAesthetic and Reconstructive Technologies, Inc.
Clearance track510(k)
Submission numberK021337
DecisionSubstantially Equivalent
Decision date2002-07-03
Date received2002-04-26
Product codeMIC
Device class2
Medical specialtyEar, Nose, Throat
Applicant locationCA, US
SourceopenFDA device

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