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

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

K Number: K013982 · Decision May 21, 2002
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
26
Applicant Total
33
Review Days
169

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Basic Information

Device Name
KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
K Number
K013982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kinamed, Inc.
Date Received
December 3, 2001
Decision Date
May 21, 2002
Product Code
KRR
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
KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

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K032950 GEM INSET PATELLAR COMPONENT
K030256 ISO-ELASTIC CERCLAGE SYSTEM
K020764 NAVIPRO
K010101 GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K003347 ORTHOPILOT
K994214 GEM KNEE SYSTEM
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