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510(k) K170654

USS System by Synthes USA Products, LLC — Product Code NKB

K170654 is an FDA 510(k) premarket notification submitted by Synthes USA Products, LLC for the device "USS System". The FDA issued a decision of Substantially Equivalent on March 29, 2017. The device falls under product code NKB (Thoracolumbosacral Pedicle Screw System), a Class II device regulated under 21 CFR 888.3070. Synthes USA Products, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 2017
Date Received
March 3, 2017
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Thoracolumbosacral Pedicle Screw System
Device Class
Class II
Regulation Number
888.3070
Review Panel
OR
Submission Type

Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.

Other clearances by Synthes USA Products, LLC

  • K180541 — DePuy Synthes 2.0 mm Quick Insertion Screws (November 21, 2018)
  • K170818 — Craniomaxillofacial Distraction System (CMFD) (December 7, 2017)
  • K162594 — Craniomaxillofacial Distraction System (CMFD) (May 8, 2017)
  • K161616 — DePuy Synthes 4.0 mm and 4.5 mm Cortex Screws, DePuy Synthes 2.4 mm Cannulated S (February 16, 2017)
  • K162358 — T-PAL Spacer System, T-PAL Titanium Spacer System, SYNFIX Evolution System (November 1, 2016)
  • K151276 — DePuy Synthes T-PAL Ti Spacer (June 18, 2015)
  • K143285 — Mandible External Fixator - MR Conditional (May 28, 2015)
  • K142838 — Synapse Occipital-Cervical-Thoracic (OCT) System (January 20, 2015)
  • K141897 — SYNAPSE SYSTEM, SYNTHES OC FUSION SYSTEM (September 25, 2014)
  • K133698 — SYNAPSE SYSTEM (January 16, 2014)

Other clearances for product code NKB

  • K261284 — Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation Sy (July 14, 2026)
  • K253802 — KHEIRON® Spinal Fixation System, including patient specific K-ROD (July 1, 2026)
  • K253045 — “Socko” Vimax Spinal Fixation System (June 17, 2026)
  • K251251 — ChanPin Pedicle Screw Spinal System (June 9, 2026)
  • K260989 — Varion Thoracolumbar Fixation System (May 15, 2026)
  • K253739 — SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® (May 7, 2026)
  • K261130 — AccelFix Spinal Fixation System (May 5, 2026)
  • K253966 — PERLA® TL Posterior Thoraco-lumbar Fixation System (May 1, 2026)
  • K252542 — LEO Spinal System (April 29, 2026)
  • K253940 — M.U.S.T. Pedicle Screw System - Extension (April 28, 2026)

FDA data resources