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

AART NASAL IMPLANT

K Number: K021418 · Decision Jul 2, 2002
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
41
Applicant Total
10
Review Days
60

Basic Information

Device Name
AART NASAL IMPLANT
K Number
K021418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC.
Date Received
May 3, 2002
Decision Date
July 2, 2002
Product Code
FZE
Advisory Committee
General, Plastic Surgery
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
FZE Prosthesis, Nose, Internal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FZE), 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
K021839 AART GLUTEAL IMPLANT
K021820 AART SILICONE CARVING BLOCK
K021337 AART PECTORALIS IMPLANT
K021419 AART MALAR IMPLANT
K021417 AART CHIN IMPLANT