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

MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE

K Number: K063487 · Decision Jan 22, 2007
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
24
Review Days
66

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Basic Information

Device Name
MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE
K Number
K063487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merete Medical GmbH
Date Received
November 17, 2006
Decision Date
January 22, 2007
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 Merete Medical GmbH

K Number Device Name
K160548 MC-Subtalar(TM) II
K152187 MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws and TwistCut Snap-Off Screws
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
Search all 24 clearances from Merete Medical GmbH →