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

ISO-ELASTIC CERCLAGE SYSTEM

K Number: K030256 · Decision Oct 21, 2003
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
33
Review Days
270

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Basic Information

Device Name
ISO-ELASTIC CERCLAGE SYSTEM
K Number
K030256
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kinamed, Inc.
Date Received
January 24, 2003
Decision Date
October 21, 2003
Product Code
JDQ
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
JDQ Cerclage, Fixation

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K Number Device Name
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K033668 NAVIPRO KNEE SOFTWARE MODULE
K032950 GEM INSET PATELLAR COMPONENT
K020764 NAVIPRO
K013982 KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
K010101 GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K003347 ORTHOPILOT
K994214 GEM KNEE SYSTEM
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