Spinal Concepts, Inc.
Spinal Concepts, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2005.
Top product codes for Spinal Concepts, Inc.
Recent clearances by Spinal Concepts, Inc.
- K051000 — FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE
- K050706 — HARMONY PORT SYSTEM, MODEL 1907 SERIES
- K040096 — SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM
- K033663 — SPINAL CONCEPTS INC. CODA
- K033517 — SPINAL CONCEPTS INC. CADENCE AND TRAXIS
- K031855 — SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM
- K031985 — SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM
- K031318 — TRAXIS CEMENT RESTRICTOR
- K031672 — SPINAL CONCEPTS, INC. INFIX SYSTEM
- K031837 — MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
- K030087 — SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM
- K031914 — SPINAL CONCEPTS, INC. CADENCE AND FORTITUDE
- K030625 — SPINAL CONCEPTS INC. PATHFINDER
- K024326 — SPINAL CONCEPTS, INC. ANT-CER DYNAMIC ANTERIOR CERVICAL PLATE SYSTEM
- K023647 — CADENCE PEEK CEMEENT RESTRICTOR
- K023644 — MODIFICATION TO INCOMPASS SPINAL FIXATION SYSTEM
- K021564 — INCOMPASS SPINAL FIXATION SYSTEM
- K021719 — FORTITUDE CEMENT RESTRICTOR
- K022218 — CADENCE CEMENT RESTRICTOR
- K021009 — OCTAFIX OCCIPITAL CERVICAL PLATING SYSTEM
- K020611 — UNIVERSAL BONE PLATE III SYSTEM (UBP III)
- K013979 — SC-ACUFIX THINLINE ANTERIOR CERVICAL PLATE SYSTEM
- K013887 — BACFIX SPINAL FIXATION SYSTEM
- K010563 — END-TO-END AND SIDE-BY-SIDE CONNECTORS
- K003351 — PARSFIX CABLE-SCREW SYSTEM
- K002082 — SPEEDLINK TRANSVERSE CONNECTOR
- K990005 — SPINAL CONCEPTS, INC. (SCI) ANTERIOR CERVICAL PLATE SYSTEM
- K983258 — MODIFICATION TO SPINAL CONCEPTS BACFIX SPINAL FIXATION SYSTEM
- K983260 — MODIFICATION TO SPINAL CONCEPTS BACFIX TI SPINAL FIXATION SYSTEM
- K973687 — SPINAL CONCEPTS, INC., BACFIX TI SPINAL FIXATION SYSTEM
- K974020 — SPINAL CONCEPTS, INC., CFIX CABLE SYSTEM
- K973586 — SPINAL CONCEPTS, INC., UNIVERSAL BONE PLATE SYSTEM II
- K964404 — BACFIX SPINAL FIXATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.