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

VSP (VARIABLE SCREW PLACEMENT)

K Number: K944736 · Decision May 5, 1995
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
41
Review Days
221

Basic Information

Device Name
VSP (VARIABLE SCREW PLACEMENT)
K Number
K944736
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ACROMED CORP.
Date Received
September 26, 1994
Decision Date
May 5, 1995
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

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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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