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

ADVANCE DOUBLE HIGH INSERT

K Number: K033890 · Decision Jan 15, 2004
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
267
Review Days
30

Basic Information

Device Name
ADVANCE DOUBLE HIGH INSERT
K Number
K033890
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WRIGHT MEDICAL TECHNOLOGY, INC.
Date Received
December 16, 2003
Decision Date
January 15, 2004
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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