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

CERAVITAL CERAMIC EAR CANAL WALL PROSTH

K Number: K813224 · Decision Apr 21, 1982
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
82
Review Days
163

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Basic Information

Device Name
CERAVITAL CERAMIC EAR CANAL WALL PROSTH
K Number
K813224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3500
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Xomed, Inc.
Date Received
November 9, 1981
Decision Date
April 21, 1982
Product Code
ESF
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
ESF Polymer, Composite Synthetic Ptfe With Carbon-Fiber, Ent

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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
K994262 FRONTAL SINUS TREPHINATION CANNULA
K992855 XPS STRAIGHTSHOT OR MODEL 2000 MICRODEBRIDER SYSTEM OR XPS POWERSCULPT
K993582 MODIFICATION TO LASER-SHIELD II
K993655 MICRO-FRANCE ELECTROSURGICAL INSTRUMENTS, VARIOUS
Search all 82 clearances from Xomed, Inc. →