Medical Device Manufacturer · FR , Bruz

Memometal Technologies - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2007

Recent clearances: MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MEMOMETAL NAVIS BONE PLATING SYSTEM, MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)

View 10 510(k) Devices ↓

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Memometal Technologies Orthopedic ✕

10 devices

1-10 of 10

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