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

REPROCESSED EXTERNAL FIXATION DEVICE

K Number: K061759 · Decision Sep 5, 2006
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
21
Review Days
75

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Basic Information

Device Name
REPROCESSED EXTERNAL FIXATION DEVICE
K Number
K061759
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ascent Healthcare Solutions
Date Received
June 22, 2006
Decision Date
September 5, 2006
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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K100537 REPROCESSED ULTRASONIC CURVED SHEARS WITH TORQUE WRENCH AND GRIP ASSIST MODEL FCS9, TWBLUE, GABLUE
K100080 REPROCESSED TROCARS, MODEL B5LT AND CB5LT
K093702 REPROCESSED ULTRASONIC COAGULATING SHEARS
K092425 REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETERS, MODEL SNDSTR10
K090323 REPROCESSED ELECTROPHYSIOLOGY CATHETERS
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