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

SUPERCABLE GRIP AND PLATE SYSTEM

K Number: K072250 · Decision Nov 9, 2007
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
33
Review Days
88

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Basic Information

Device Name
SUPERCABLE GRIP AND PLATE SYSTEM
K Number
K072250
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinamed, Inc.
Date Received
August 13, 2007
Decision Date
November 9, 2007
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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Other Clearances by Kinamed, Inc.

K Number Device Name
K122049 NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM
K050897 NAVIPRO SHOULDER SOFTWARE MODULE
K033668 NAVIPRO KNEE SOFTWARE MODULE
K032950 GEM INSET PATELLAR COMPONENT
K030256 ISO-ELASTIC CERCLAGE SYSTEM
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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