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

GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT

K Number: K032295 · Decision Aug 21, 2003
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
529
Review Days
27

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Basic Information

Device Name
GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT
K Number
K032295
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew, Inc.
Date Received
July 25, 2003
Decision Date
August 21, 2003
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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