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

FX-CABLELOK(TM) STOP(TROCHANTER HOOK) SYSTEM

K Number: K935646 · Decision Mar 9, 1994
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
30
Review Days
106

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Basic Information

Device Name
FX-CABLELOK(TM) STOP(TROCHANTER HOOK) SYSTEM
K Number
K935646
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Biodynamic Technologies, Inc.
Date Received
November 23, 1993
Decision Date
March 9, 1994
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

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K990513 ULTIMAX CORTICAL BONE SCREWS
K981230 ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
K980102 BTI HUMERAL INTRAMEDULLARY ROD SYSTEM
K974756 BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS
K972403 BTI CORTICAL BONE SCREWS
K970897 BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
K962706 EZ-FIX CANNULATED SCREW SYSTEM
K962987 EZ-FIX SMALL CANNULATED SCREW SYSTEM
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