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

NOVATION SPLINED RDD FEMORAL STEMS

K Number: K063279 · Decision Nov 29, 2006
Classifications
1
FEI Numbers
284
Registration Numbers
284
Same Product Code
522
Applicant Total
146
Review Days
29

Basic Information

Device Name
NOVATION SPLINED RDD FEMORAL STEMS
K Number
K063279
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EXACTECH, INC.
Date Received
October 31, 2006
Decision Date
November 29, 2006
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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