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

ISOLA ANTERIOR SYSTEM

K Number: K943819 · Decision Feb 9, 1995
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
41
Review Days
188

Basic Information

Device Name
ISOLA ANTERIOR SYSTEM
K Number
K943819
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
August 5, 1994
Decision Date
February 9, 1995
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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Other Clearances by ACROMED CORP.

K Number Device Name
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K981274 ACROMED TIMX PLATE BASED LOW BACK SYSTEM
K980228 UNIVERSITY PLATE ANTERIOR SYSTEM
K974757 KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
K972718 M-2 ANTERIOR PLATE SYSTEM
K970955 ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
K971248 KANEDA SR ANTERIOR SPINAL SYSTEM
K970950 EASY ROD
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