FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

PICCOLO COMPOSITE ANKLE ARTHRODESIS NAILING SYSTEM

K Number: K123810 · Decision Jun 14, 2013
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
32
Review Days
185

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Basic Information

Device Name
PICCOLO COMPOSITE ANKLE ARTHRODESIS NAILING SYSTEM
K Number
K123810
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CarboFix Orthopedics , Ltd.
Date Received
December 11, 2012
Decision Date
June 14, 2013
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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Other Clearances by CarboFix Orthopedics , Ltd.

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K240846 CarboClear® Hybrid Pedicle Screw System; CarboClear® Hybrid Navigated Instruments; CarboClear® Hybrid Fenestrated Pedicle Screw System and High V+® Bone Cement; CarboClear® X Fenestrated Pedicle Screw System and High V+® Bone Cement
K233989 CarboClear® Posterior Cervical Screw System
K233944 CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments
K232341 CarboClear® Pedicle Screw System
K231280 CarboClear® X Pedicle Screw System; CarboClear® X Navigated Instruments; CarboClear® X Fenestrated Pedicle Screw System with High V+® Bone Cement
K210716 CarboClear X Pedicle Screw System, CarboClear X Navigated Instruments
K203317 CarboClear X Pedicle Screw System
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