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

MERETE COMPRESSION SCREWS

K Number: K091798 · Decision Sep 2, 2009
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
24
Review Days
77

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Basic Information

Device Name
MERETE COMPRESSION SCREWS
K Number
K091798
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merete Medical GmbH
Date Received
June 17, 2009
Decision Date
September 2, 2009
Product Code
HWC
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
HWC Screw, Fixation, Bone

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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 →