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

OSTEOBRIDGE IKA INTRAMEDULLARY KNEE ARTHRODESIS ROD FIXATION SYSTEM

K Number: K101939 · Decision Oct 7, 2010
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
24
Review Days
87

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Basic Information

Device Name
OSTEOBRIDGE IKA INTRAMEDULLARY KNEE ARTHRODESIS ROD FIXATION SYSTEM
K Number
K101939
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merete Medical GmbH
Date Received
July 12, 2010
Decision Date
October 7, 2010
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 Merete Medical GmbH

K Number Device Name
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K151762 PediatrOS RigidTack/FlexTack
K142451 OsteoBridge IDSF - Intramedullary Diaphyseal Segmental Defect Fixation Rod System
K141377 BIOBALL DELTA CERAMIC HEADS, MULTICUP PE INLAY STANDARD
K140069 LOCKING BONE PLATE STYLE 14, METAFIX LOCKING SCREW 3.8, MERETE CANNULATED PCS 3.0
K132226 METAFIX BLP PLATE, SIZE 31, LEFT, METAFIX BLP PLATE, SIZE 31,RIGHT
K123619 INTRABLOCK BIOBALL HIP SYSTEM (IBS)
K130400 MERETEC CS, CORTICAL SCREWS
K120787 MERETE LOCKING BONE PLATE SYSTEM III
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