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

SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)

K Number: K955173 · Decision Feb 9, 1996
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
24
Review Days
88

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Basic Information

Device Name
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
K Number
K955173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Osteotech, Inc.
Date Received
November 13, 1995
Decision Date
February 9, 1996
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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K081227 PLEXUR M
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K073405 PLEXUR M
K061982 PLEXUR P
K051188 GRAFTON DBM
K051781 GRAFTCAGE TLX
K051195 GRAFTON DBM
K043209 VIAGRAF DBM PASTE
K053080 GRAFTCAGE ACX
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