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

ISOLA(R) TANDEM CONNECTOR

K Number: K922504 · Decision May 18, 1993
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
41
Review Days
356

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Basic Information

Device Name
ISOLA(R) TANDEM CONNECTOR
K Number
K922504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Acromed Corp.
Date Received
May 27, 1992
Decision Date
May 18, 1993
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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Other Clearances by Acromed Corp.

K Number Device Name
K980485 ISOLA SPINAL SYSTEM
K981714 TIMX LOW BACK SYSTEM TITANIUM MX ROD BASED LOW BACK 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
Search all 41 clearances from Acromed Corp. →