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

BALANCED KNEE SYSTEM REVISION OFFSET TIBIA

K Number: K103837 · Decision Mar 24, 2011
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
5
Review Days
84

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Basic Information

Device Name
BALANCED KNEE SYSTEM REVISION OFFSET TIBIA
K Number
K103837
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Development
Date Received
December 30, 2010
Decision Date
March 24, 2011
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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