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

ORTHOMET RESURFACING FEMORAL COMPONENT

K Number: K944752 · Decision Dec 28, 1994
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
22
Applicant Total
60
Review Days
93

Basic Information

Device Name
ORTHOMET RESURFACING FEMORAL COMPONENT
K Number
K944752
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3400
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthomet, Inc.
Date Received
September 26, 1994
Decision Date
December 28, 1994
Product Code
KXA
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
KXA Prosthesis, Hip, Femoral, Resurfacing

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