Search FDA 510(k) Devices

4,872 clearances indexed · Search by device name, K-number, manufacturer or product code

57 results for "Spine Wave, Inc."
49–57 of 57
Cleared Sep 03, 2009
STAXX XD SYSTEM
K090315 · MQP
Spine Wave, Inc.
Orthopedic · 206d
Cleared Jan 13, 2009
CAPSURE PS SYSTEM
K083743 · MNI
Spine Wave, Inc.
Orthopedic · 28d
Cleared Dec 11, 2008
CAPSURE(R) PS SYSTEM
K083353 · MNI
Spine Wave, Inc.
Orthopedic · 28d
Cleared May 12, 2008
CAPSURE PS (R) SPINE SYSTEM
K081228 · MNI
Spine Wave, Inc.
Orthopedic · 12d
Cleared Apr 13, 2007
MODIFICATION TO STAXX FX SYSTEM
K063606 · OBL
Spine Wave, Inc.
Orthopedic · 133d
Cleared Apr 05, 2007
CAPSURE PEDICLE SCREW SYSTEM
K070245 · MNI
Spine Wave, Inc.
Orthopedic · 70d
Cleared Jul 03, 2006
STAXX FX SYSTEM
K053336 · NDN
Spine Wave, Inc.
Orthopedic · 214d
Cleared Apr 27, 2006
STAXX XD SYSTEM
K052670 · MQP
Spine Wave, Inc.
Orthopedic · 212d
Cleared Jun 24, 2004
WAFER SYSTEM
K033303 · HRS
Spine Wave, Inc.
Orthopedic · 254d