Memometal Technologies is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Memometal Technologies - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Memometal Technologies has 10 FDA 510(k) cleared orthopedic devices. Based in Bruz, FR.
Historical record: 10 cleared submissions from 2007 to 2011.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Memometal Technologies
10 devices
Cleared
Nov 17, 2011
MEMOMETAL INTRA-MEDULLARY BONE FASTENER
Orthopedic
108d
Cleared
Mar 15, 2011
MEMOMETAL NAVIS BONE PLATING SYSTEM
Orthopedic
249d
Cleared
Nov 03, 2010
MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)
Orthopedic
103d
Cleared
May 19, 2010
SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115
Orthopedic
156d
Cleared
Feb 06, 2009
MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL,...
Orthopedic
77d
Cleared
Dec 04, 2007
MEMOMETAL BONE ANCHORS
Orthopedic
144d
Cleared
Jul 26, 2007
MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE
Orthopedic
146d
Cleared
Mar 21, 2007
MEMOMETAL FIXOS SCREWS
Orthopedic
77d
Cleared
Mar 19, 2007
MEMOMETAL MEMORY STAPLES
Orthopedic
75d
Cleared
Mar 19, 2007
MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10
Orthopedic
75d