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

EBI XFIX DFS SYSTEM

K Number: K022319 · Decision Aug 12, 2002
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
95
Review Days
26

Basic Information

Device Name
EBI XFIX DFS SYSTEM
K Number
K022319
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EBI, L.P.
Date Received
July 17, 2002
Decision Date
August 12, 2002
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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