510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K021337Substantially Equivalent

Aart Pectoralis Implant

Aesthetic and Reconstructive Technologies, Inc., Paso Robles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K021337 is the FDA 510(k) clearance record for AART PECTORALIS IMPLANT, a class II device, cleared for Aesthetic and Reconstructive Technologies, Inc. on under FDA product code MIC (Implant, Muscle, Pectoralis). FDA records list 10 510(k) clearances for Aesthetic and Reconstructive Technologies, Inc., from to . As of , FDA records show one recall naming K021337.

Clearance record

Decision date
Received
(68 days to decision)
Product code
MIC Implant, Muscle, Pectoralis
Regulation
21 CFR 874.3620
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Aesthetic and Reconstructive Technologies, Inc. 5871 Lone Pine Pl., Paso Robles CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MIC

Trailing 12 months

FDA records hold no clearances under product code MIC in the trailing twelve months.

FDA records show no clearances under product code MIC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MIC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260