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

MICROTEK TOTAL OSSICULAR PROTHESIS

K Number: K895815 · Decision Dec 26, 1989
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
38
Applicant Total
13
Review Days
88

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Basic Information

Device Name
MICROTEK TOTAL OSSICULAR PROTHESIS
K Number
K895815
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3495
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Microbio-Medics, Inc.
Date Received
September 29, 1989
Decision Date
December 26, 1989
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ETA), ordered by most recent decision date.

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Other Clearances by Microbio-Medics, Inc.

K Number Device Name
K923353 VENTILATION TUBES W/ HYDROGEL COATING
K922572 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR
K913276 MICROTEK MEDICAL'S SOUND STIKS
K904239 SOFT HYDROXYLAPATITE OSSICULAR MALLEABLE PROSTHES
K910167 MICROTEK-HERITAGES SILICONE BULB EVACUATION SYSTEM
K900726 MICROTEK MEDICAL'S BLOOD COLLECTION KIT
K901154 MICROTEK'S SURGICAL LAMP HANDLE & COVER
K895814 MICROTEK PISTON & WIRE PROSTHESES
K895502 MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT
K885201 OSSICULAR PROSTHESES 4 PARTIAL, 4 TOTAL, 2 CONVERT
Search all 13 clearances from Microbio-Medics, Inc. →