Abbott Spine, Inc.
Abbott Spine, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2009.
Top product codes for Abbott Spine, Inc.
Recent clearances by Abbott Spine, Inc.
- K090060 — NEXLINK OCT SYSTEM, MODEL 7000 SERIES
- K082032 — SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310)
- K081622 — UNIVERSAL CLAMP STAINLESS STEEL SYSTEM
- K073202 — ARDIS SPACER
- K072672 — SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
- K071174 — PATHFINDER SYSTEM POLYAXIAL PEDICLE SCREWS
- K062505 — NEX-LINK SPINAL FIXATION SYSTEM OFFSET CONNECTORS, 2121-XX SERIES
- K060634 — NEX-LINK SPINAL FIXATION SYSTEM ROD TO ROD CONNECTORS, MODELS 725, 726 SERIES
- K060009 — ABBOTT SPINE UNIVERSAL CLAMP SYSTEM
- K052566 — NEX-LINK SPINAL FIXATION SYSTEM OPEN POLYAXIAL SCREWS, MODELS 2112, 2113, 2118, 2119, 2120. NEX-LINK SPINAL FIXATION SY
- K052638 — ABBOTT SPINE, INC. SPINNAKER SYSTEM
- K052247 — NEX-LINK SPINAL FIXATION SYSTEM VARIABLE CROSSLINK, MODEL 721-XX
- K052072 — THE SC-ACUFIX ANT-CER DYNAMIC CERVICAL PLATE SYSTEM SINGLE LEVEL PLATES
Data sourced from openFDA. This site is unofficial and independent of the FDA.