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

DISTAL CENTRALIZER, EXETER II HIP SYSTEM

K Number: K974054 · Decision Dec 23, 1997
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
560
Applicant Total
36
Review Days
57

Basic Information

Device Name
DISTAL CENTRALIZER, EXETER II HIP SYSTEM
K Number
K974054
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOWMEDICA, INC.
Date Received
October 27, 1997
Decision Date
December 23, 1997
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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