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

REJUVENATE MONOLITHIC HIP SYSTEM

K Number: K082892 · Decision Dec 29, 2008
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
157
Applicant Total
78
Review Days
90

Basic Information

Device Name
REJUVENATE MONOLITHIC HIP SYSTEM
K Number
K082892
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOWMEDICA OSTEONICS CORP
Date Received
September 30, 2008
Decision Date
December 29, 2008
Product Code
MEH
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
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

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