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

VERSA-FX FEMORAL FIXATION SYSTEM

K Number: K954555 · Decision Jan 26, 1996
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
376
Review Days
116

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Basic Information

Device Name
VERSA-FX FEMORAL FIXATION SYSTEM
K Number
K954555
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer, Inc.
Date Received
October 2, 1995
Decision Date
January 26, 1996
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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