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

TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM

K Number: K981714 · Decision Jun 30, 1998
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
41
Review Days
46

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Basic Information

Device Name
TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK SYSTEM
K Number
K981714
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
May 15, 1998
Decision Date
June 30, 1998
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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Other Clearances by Acromed Corp.

K Number Device Name
K980485 ISOLA SPINAL SYSTEM
K981113 PEDIATRIC PRC
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
K971248 KANEDA SR ANTERIOR SPINAL SYSTEM
K970955 ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
K970950 EASY ROD
K965102 ACROMED PEDICLE SCREW
Search all 41 clearances from Acromed Corp. →