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

TRIAD II MODULAR TOTAL HIP SYSTEM

K Number: K003199 · Decision Jan 10, 2001
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
21
Review Days
90

Basic Information

Device Name
TRIAD II MODULAR TOTAL HIP SYSTEM
K Number
K003199
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
OSTEOIMPLANT TECHNOLOGY, INC.
Date Received
October 12, 2000
Decision Date
January 10, 2001
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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