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

CHIBA SPINAL SYSTEM

K Number: K895978 · Decision Aug 9, 1990
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
56
Review Days
301

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Basic Information

Device Name
CHIBA SPINAL SYSTEM
K Number
K895978
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Danek Medical, Inc.
Date Received
October 12, 1989
Decision Date
August 9, 1990
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 Danek Medical, Inc.

K Number Device Name
K994122 BONE GRAFT WASHER, MODEL 9090114 - 9090118
K993810 CD HORIZON SPINAL SYSTEM
K993855 ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
K991528 MODIFICATION TO TENOR SPINAL SYSTEM-ROD/BOLT CONNECTOR
K990603 MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM
K982875 MODIFICATION TO ZPLATE-ATL ANTERIOR FIXATION SYSTEM
K984522 MODIFICATION OF TSRH SPINAL SYSTEM
K982154 MODIFICATION OF TOWNLEY PEDICLE SCREW PLATING SYSTEM
K970599 TOWNLEY PEDICLE SCREW PLATING SYSTEM
K943827 SPINE FIXATION
Search all 56 clearances from Danek Medical, Inc. →