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

KANEDA SR ANTERIOR SPINAL SYSTEM

K Number: K971248 · Decision Jun 11, 1997
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
41
Review Days
69

Basic Information

Device Name
KANEDA SR ANTERIOR SPINAL SYSTEM
K Number
K971248
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
April 3, 1997
Decision Date
June 11, 1997
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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