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

CERAVITAL CERAMIC OSSICULAR REPL. PROS.

K Number: K810707 · Decision Jun 16, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
37
Applicant Total
82
Review Days
92

Basic Information

Device Name
CERAVITAL CERAMIC OSSICULAR REPL. PROS.
K Number
K810707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3495
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
XOMED, INC.
Date Received
March 16, 1981
Decision Date
June 16, 1981
Product Code
ETA
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ETA Replacement, Ossicular Prosthesis, Total

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K Number Device Name
K002395 MODEL 30 CLASSIC PNEUMATONOMETER
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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
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