Home / 510(k) Clearances / K250305

510(k) K250305

Reprocessed Agilis NxT Steerable Introducer by Innovative Health — Product Code PNE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 7, 2026
Date Received
February 3, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reprocessed Catheter Introducer
Device Class
Class II
Regulation Number
870.1340
Review Panel
CV
Submission Type

Introduce various cardiovascular catheters into the heart and cardiovascular system

Other clearances by Innovative Health

  • K231015 — Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters (July 1, 2024)
  • K233825 — Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter (June 7, 2024)
  • K232037 — Reprocessed VersaCross Steerable Sheath; Reprocessed SureFlex Steerable Guiding (April 4, 2024)
  • K230376 — Reprocessed Agilis NxT Steerable Introducer (August 7, 2023)
  • K213584 — Reprocessed NRG Transseptal Needle (April 4, 2023)
  • K221854 — Reprocesses Umbilical Cable (August 6, 2022)
  • K210655 — Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter (May 25, 2022)
  • K212165 — Reprocessed Carto Vizigo Bi-Directional Guiding Sheath (March 10, 2022)
  • K212776 — Reprocessed Advisor HD Grid Mapping Catheter, Sensor Enabled (December 20, 2021)
  • K211662 — Reprocessed IntellaMap Orion High Resolution Mapping Catheter (November 18, 2021)

Other clearances for product code PNE

  • K250314 — Medline ReNewal Reprocessed Abbott Agilis Nxt Steerable Introducer (December 19, 2025)
  • K232037 — Reprocessed VersaCross Steerable Sheath; Reprocessed SureFlex Steerable Guiding (April 4, 2024)
  • K230376 — Reprocessed Agilis NxT Steerable Introducer (August 7, 2023)
  • K212165 — Reprocessed Carto Vizigo Bi-Directional Guiding Sheath (March 10, 2022)
  • K170311 — Reprocessed Agilis NxT Steerable Introducer (June 2, 2017)
  • K152090 — Reprocessed Steerable Introducer (March 23, 2016)