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

DURALASTIC ANATOMICAL NASAL IMPLANTS

K Number: K973573 · Decision Nov 13, 1997
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
41
Applicant Total
14
Review Days
55

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Basic Information

Device Name
DURALASTIC ANATOMICAL NASAL IMPLANTS
K Number
K973573
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
Hanson Medical, Inc.
Date Received
September 19, 1997
Decision Date
November 13, 1997
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 Hanson Medical, Inc.

K Number Device Name
K141822 SENSEI X ROBOTIC CATHETER SYSTEM
K090803 HANSON MEDICAL FACIAL IMPLANTS
K071018 MONARCH NASAL IMPLANT
K041690 MONARCH NASAL IMPLANT
K040307 HANSON SCAR ADE
K030808 HANSON MEDICAL CALF IMPLANT
K030809 HANSON MEDICAL GLUTEAL IMPLANT
K973730 DURASIL I AND DURASIL II
K973729 POWERFLEX PEC IMPLANT
K973728 SILICONE CARVING BLOCK
Search all 14 clearances from Hanson Medical, Inc. →