FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AART PECTORALIS IMPLANT

K Number: K021337 · Decision Jul 3, 2002
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
7
Applicant Total
10
Review Days
68

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Basic Information

Device Name
AART PECTORALIS IMPLANT
K Number
K021337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesthetic and Reconstructive Technologies, Inc.
Date Received
April 26, 2002
Decision Date
July 3, 2002
Product Code
MIC
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MIC Implant, Muscle, Pectoralis

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MIC), ordered by most recent decision date.

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Other Clearances by Aesthetic and Reconstructive Technologies, Inc.

K Number Device Name
K023678 DIMISIL SCAR GEL
K022306 AART SILICONE TUBING
K022511 AART CALF IMPLANT
K022223 AART SILICONE SHEETING
K021820 AART SILICONE CARVING BLOCK
K021839 AART GLUTEAL IMPLANT
K021417 AART CHIN IMPLANT
K021419 AART MALAR IMPLANT
K021418 AART NASAL IMPLANT