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

IMPLANTECH DORSAL NASAL IMPLANT

K Number: K942876 · Decision Jul 18, 1994
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
41
Applicant Total
34
Review Days
31

Basic Information

Device Name
IMPLANTECH DORSAL NASAL IMPLANT
K Number
K942876
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
IMPLANTECH ASSOCIATES, INC.
Date Received
June 17, 1994
Decision Date
July 18, 1994
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

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Other Clearances by IMPLANTECH ASSOCIATES, INC.

K Number Device Name
K013732 GELZONE
K012419 CONFORM SHEETING, MODEL IGEL
K002886 IMPLANTECH COMPOSITE FACIAL IMPLANTS (MALAR, CHIN, AND NASAL)
K973502 IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT
K964846 IMPLATECH RP MEDICAL GRADE SILICONE GEL SHEETING
K962824 IMPLANTECH JEJ PERI-PYRIFORM IMPLANT
K962261 IMPLANTECH WM NASAL-LABIAL IMPLANT
K943988 IMPLANTECH NASAL LABIAL IMPLANT
K943644 IMPLANTECH TEMPORAL IMPLANT
K941960 IMPLANTECH DORSAL COLUMELLA IMPLANT STYLE II
Search all 34 clearances from IMPLANTECH ASSOCIATES, INC. →