Spinecraft, LLC
FDA 510(k) medical device clearances.
Top product codes for Spinecraft, LLC
Recent clearances by Spinecraft, LLC
- K223301 — ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System
- K223273 — ASTRA Spine System
- K211935 — ORIO-Ti Intervertebral Body Fusion Cage System
- K211323 — ASTRA Spine System
- K181350 — ASTRA-OCT Spine System
- K143683 — APEX-DL Spine System
- K150417 — ASTRA SPINE SYSTEM
- K131521 — VELOX ANTERIOR CERVICAL PLATE SYSTEM
- K132603 — APEX SPINE SYSTEM
- K110906 — APEX SPINE SYSTEM
- K103505 — ALTUM ANTERIOR CERVICAL PLATE
- K102488 — APEX SPINE SYSTEM W/ COCR RODS
Data sourced from openFDA. This site is unofficial and independent of the FDA.