Memometal Technologies

10 FDA 510(k) medical device clearances.

Top product codes for Memometal Technologies

Recent clearances by Memometal Technologies

K112197 — MEMOMETAL INTRA-MEDULLARY BONE FASTENER HTY · 2011-11-17
K101930 — MEMOMETAL NAVIS BONE PLATING SYSTEM HRS · 2011-03-15
K102072 — MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE) HTY · 2010-11-03
K093820 — SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115 HWC · 2010-05-19
K083447 — MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50 HRS · 2009-02-06
K071941 — MEMOMETAL BONE ANCHORS HWC · 2007-12-04
K070598 — MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE HTY · 2007-07-26
K070039 — MEMOMETAL FIXOS SCREWS HWC · 2007-03-21
K070031 — MEMOMETAL MEMORY STAPLES JDR · 2007-03-19
K070033 — MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 JDR · 2007-03-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.