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

AUTOGENESIS(TM) AUTOMATOR

K Number: K905514 · Decision Apr 2, 1991
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
22
Review Days
116

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Basic Information

Device Name
AUTOGENESIS(TM) AUTOMATOR
K Number
K905514
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Advanced Biosearch Assn.
Date Received
December 7, 1990
Decision Date
April 2, 1991
Product Code
KTT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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