Precision Spine, Inc.
Precision Spine, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2025.
Top product codes for Precision Spine, Inc.
Recent clearances by Precision Spine, Inc.
- K250769 — Dakota LP System
- K242297 — Reform Pedicle Screw System
- K231229 — S-COMP Reform® POCT Navigation Instruments
- K220862 — E-GPS Navigated Instruments
- K213118 — Dakota ALIF System
- K220324 — AccuFit Lateral 2-Hole Plate
- K212075 — ShurFit Lumbar Interbody System
- K212937 — Dakota ALIF Plate System
- K203129 — NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System
- K181606 — Precision Spine Navigation Instrumentation
- K172495 — Reform® POCT System
- K173130 — Reform® Midline Cortical Screw System
- K171657 — ShurFit 2C Lumbar Interbody Fusion System
- K161809 — ShurFit CpTi-HA ACIF Interbody Fusion System
- K162211 — AccuFit Lateral Plate System
- K162300 — Reform® POCT System
- K160568 — Precision Spine Interspinous Plate System
- K151422 — Reform Pedicle Screw System
- K151863 — Precision Spine Interspinous Plate System
- K150856 — Reform Pedicle Screw System
- K150851 — Sure Lok Mini Posterior Cervical/Upper Thoracic System
- K143248 — Reform Pedicle Screw System
- K142378 — Interspinous Plate System
- K141397 — SURE-LOK C EXTENDED TAB PEDICLE SCREW SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.