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