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

SPINAL CONCEPTS, INC., CFIX CABLE SYSTEM

K Number: K974020 · Decision Dec 19, 1997
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
33
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SPINAL CONCEPTS, INC., CFIX CABLE SYSTEM
K Number
K974020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Concepts, Inc.
Date Received
October 22, 1997
Decision Date
December 19, 1997
Product Code
JDQ
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
JDQ Cerclage, Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JDQ), ordered by most recent decision date.

View all

Other Clearances by Spinal Concepts, Inc.

K Number Device Name
K051000 FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE
K050706 HARMONY PORT SYSTEM, MODEL 1907 SERIES
K040096 SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM
K033663 SPINAL CONCEPTS INC. CODA
K033517 SPINAL CONCEPTS INC. CADENCE AND TRAXIS
K031855 SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM
K031985 SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM
K031318 TRAXIS CEMENT RESTRICTOR
K031672 SPINAL CONCEPTS, INC. INFIX SYSTEM
K031837 MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
Search all 33 clearances from Spinal Concepts, Inc. →