FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FRONTAL SINUS TREPHINATION CANNULA

K Number: K994262 · Decision Feb 8, 2000
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
18
Applicant Total
82
Review Days
53

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Basic Information

Device Name
FRONTAL SINUS TREPHINATION CANNULA
K Number
K994262
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xomed, Inc.
Date Received
December 17, 1999
Decision Date
February 8, 2000
Product Code
KAM
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
KAM Cannula, Sinus

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Other Clearances by Xomed, Inc.

K Number Device Name
K002395 MODEL 30 CLASSIC PNEUMATONOMETER
K002987 REDTRONIC XOMED MONOPOLAR ENERGIZED BLADE
K002828 XPS NITRO SYSTEM
K002897 TITANIUM MIDDLE EAR PROSTHESES
K993653 MICRO-FRANCE TROCARS AND ACCESSORIES
K001148 MEROGEL OTOLOGIC PACK
K992855 XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
K993582 MODIFICATION TO LASER-SHIELD II
K993655 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
K993112 XOMED ENT RF SYSTEM
Search all 82 clearances from Xomed, Inc. →