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

MPACT ACETABULAR SYSTEM

K Number: K103721 · Decision Mar 21, 2011
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
37
Review Days
90

Basic Information

Device Name
MPACT ACETABULAR SYSTEM
K Number
K103721
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDACTA INTERNATIONAL
Date Received
December 21, 2010
Decision Date
March 21, 2011
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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