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

FREEMAN TOTAL HIP SYSTEM RIDGED STEM

K Number: K890331 · Decision Oct 13, 1989
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
80
Applicant Total
95
Review Days
263

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Basic Information

Device Name
FREEMAN TOTAL HIP SYSTEM RIDGED STEM
K Number
K890331
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3360
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Systems, Inc.
Date Received
January 23, 1989
Decision Date
October 13, 1989
Product Code
LWJ
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
LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

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K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K895217 CORTICAL SCREW
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