Medical Device Manufacturer · US , Round Rock , TX

Medicrea Technologies - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2007
14
Total
14
Cleared
0
Denied

Medicrea Technologies has 14 FDA 510(k) cleared orthopedic devices. Based in Round Rock, US.

Historical record: 14 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 - Medicrea Technologies
14 devices
1-14 of 14
Cleared Aug 23, 2011
PASS ANTERIOR SPINAL SYSTEM
K102406 · KWQ
Orthopedic · 364d
Cleared Jul 22, 2010
IMPIX LUMBAR INTERBODY DEVICE
K100544 · MAX
Orthopedic · 147d
Cleared May 19, 2010
IMPIX ALIF LUMBAR IBF, IMPIX ALIF-D LUMBAR IBF, IMPIX TLIF LUMBAR IBF
K083798 · MAX
Orthopedic · 513d
Cleared Mar 04, 2010
PASS LP SPINAL SYSTEM
K100297 · MNI
Orthopedic · 30d
Cleared Jul 31, 2009
PASS LP SPINAL SYSTEM
K083810 · MNI
Orthopedic · 221d
Cleared Dec 10, 2008
PASS LP SPINAL SYSTEM
K083308 · MNI
Orthopedic · 30d
Cleared Oct 03, 2008
PASS 2 SPINAL SYSTEM
K082069 · MNI
Orthopedic · 73d
Cleared Oct 03, 2008
PASS LP SPINAL SYSTEM
K082577 · MNH
Orthopedic · 28d
Cleared Apr 09, 2008
PASS SPINAL SYSTEM
K080099 · MNI
Orthopedic · 86d
Cleared Dec 10, 2007
IMPIX SPACER
K072226 · MAX
Orthopedic · 122d
Cleared Oct 18, 2007
MODIFICATION TO PASSMED SPINAL SYSTEM
K070530 · MNH
Orthopedic · 237d
Cleared Sep 21, 2007
MODIFICATION TO PASSMED SPINAL SYSTEM
K070276 · MNI
Orthopedic · 235d
Cleared Aug 03, 2007
C-JAWS CERVICAL COMPRESSIVE MINI FRAME
K072040 · KWQ
Orthopedic · 9d
Cleared Jan 16, 2007
C-JAWS CERVICAL COMPRESSIVE MINI FRAME
K062181 · KWP
Orthopedic · 169d
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