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

ORTHOMET ACETABULAR CUP SYSTEM

K Number: K931333 · Decision Oct 14, 1994
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
60
Review Days
577

Basic Information

Device Name
ORTHOMET ACETABULAR CUP SYSTEM
K Number
K931333
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ORTHOMET, INC.
Date Received
March 16, 1993
Decision Date
October 14, 1994
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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