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FDA 510(k) Application Details - K021418
Device Classification Name
Prosthesis, Nose, Internal
More FDA Info for this Device
510(K) Number
K021418
Device Name
Prosthesis, Nose, Internal
Applicant
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC.
3545 AIRWAY DR.
SUITE 108
RENO, NV 89511 US
Other 510(k) Applications for this Company
Contact
CATHERINE RIPLE
Other 510(k) Applications for this Contact
Regulation Number
878.3680
More FDA Info for this Regulation Number
Classification Product Code
FZE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/03/2002
Decision Date
07/02/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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