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

SYNTHES SMALL EXTERNAL FIXATION SYSTEM, SYNTHES LARGE EXTERNAL FIXATION SYSTEM

K Number: K122455 · Decision Apr 11, 2013
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
11
Review Days
241

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Basic Information

Device Name
SYNTHES SMALL EXTERNAL FIXATION SYSTEM, SYNTHES LARGE EXTERNAL FIXATION SYSTEM
K Number
K122455
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes
Date Received
August 13, 2012
Decision Date
April 11, 2013
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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Other Clearances by Synthes

K Number Device Name
K123723 SYNTHES MATRIXNEURO CRANIAL PLATING SYSTEM
K113071 SYNTHECEL DURA REPLACEMENT DEVICES
K110604 VBB SYSTEM
K093772 SYNTHES STERNAL FIXATION SYSTEM
K013072 CHRONOS TRICALCIUM PROSPHATE (CHRONOS TCP)
K020602 SYNTHES PILON PLATE
K010108 USS-LINE EXTENSION
K003836 SYNTHES SYNEX SPACER SYSTEM
K003061 SYNTHES USS (10.0MM SIDE OPENING SCREWS)
K982732 SYNTHES (USA) DISTAL RADIUS PLATE SYSTEM (DRPS)
Search all 11 clearances from Synthes →