Merete Medical GmbH - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Merete Medical GmbH has 24 FDA 510(k) cleared orthopedic devices. Based in New York, US.
Historical record: 24 cleared submissions from 2005 to 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
24 devices
Cleared
Apr 29, 2016
MC-Subtalar(TM) II
Orthopedic
60d
Cleared
Feb 12, 2016
MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws,...
Orthopedic
191d
Cleared
Dec 28, 2015
PediatrOS RigidTack/FlexTack
Orthopedic
182d
Cleared
Feb 09, 2015
OsteoBridge IDSF - Intramedullary Diaphyseal Segmental Defect Fixation Rod...
Orthopedic
160d
Cleared
Nov 21, 2014
BIOBALL DELTA CERAMIC HEADS, MULTICUP PE INLAY STANDARD
Orthopedic
178d
Cleared
Apr 07, 2014
LOCKING BONE PLATE STYLE 14, METAFIX LOCKING SCREW 3.8, MERETE CANNULATED PCS...
Orthopedic
84d
Cleared
Aug 09, 2013
METAFIX BLP PLATE, SIZE 31, LEFT, METAFIX BLP PLATE, SIZE 31,RIGHT
Orthopedic
23d
Cleared
May 24, 2013
INTRABLOCK BIOBALL HIP SYSTEM (IBS)
Orthopedic
182d
Cleared
Apr 05, 2013
MERETEC CS, CORTICAL SCREWS
Orthopedic
45d
Cleared
Nov 27, 2012
MERETE LOCKING BONE PLATE SYSTEM III
Orthopedic
257d
Cleared
May 02, 2012
OSTEOBRIDGE IKA KNEE ARTHODESIS NAIL WITH COLLAR
Orthopedic
30d
Cleared
Dec 09, 2011
OSLEOBRIDGE IDSF SPACER CONECTOR
Orthopedic
30d