Abbott Spine, Inc.
FDA 510(k) medical device clearances.
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.