Medical Device Manufacturer · US , Austin , TX

Abbott Spine, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2005

Recent clearances: NEX-LINK SPINAL FIXATION SYSTEM OPEN POLYAXIAL SCREWS, MODELS 2112, 2113, 2118, 2119, 2120. NEX-LINK SPINAL FIXATION SY, ABBOTT SPINE, INC. SPINNAKER SYSTEM, NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX

13
Total
13
Cleared
0
Denied

Abbott Spine, Inc. has 13 FDA 510(k) cleared orthopedic devices. Based in Austin, US.

Historical record: 13 cleared submissions from 2005 to 2009.

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 - Abbott Spine, Inc.

13 devices
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