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

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS

K Number: K974757 · Decision Mar 5, 1998
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
41
Review Days
76

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Basic Information

Device Name
KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
K Number
K974757
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Acromed Corp.
Date Received
December 19, 1997
Decision Date
March 5, 1998
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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K Number Device Name
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K981113 PEDIATRIC PRC
K981274 ACROMED TIMX PLATE BASED LOW BACK SYSTEM
K980228 UNIVERSITY PLATE ANTERIOR SYSTEM
K972718 M-2 ANTERIOR PLATE SYSTEM
K971248 KANEDA SR ANTERIOR SPINAL SYSTEM
K970955 ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
K970950 EASY ROD
K965102 ACROMED PEDICLE SCREW
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