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

Eminent Foot Plate System

K Number: K143365 · Decision Mar 30, 2015
Classifications
1
FEI Numbers
505
Registration Numbers
505
Same Product Code
1254
Applicant Total
5
Review Days
126

Basic Information

Device Name
Eminent Foot Plate System
K Number
K143365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eminent Spine
Date Received
November 24, 2014
Decision Date
March 30, 2015
Product Code
HRS
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
HRS Plate, Fixation, Bone

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K221936 Standalone ALIF Interbody Fusion System