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510(k) K243503

VIA360™ Surgical System by New World Medical, Inc. — Product Code MRH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 14, 2025
Date Received
November 12, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion, Ophthalmic
Device Class
Class II
Regulation Number
880.5725
Review Panel
OP
Submission Type

Other clearances by New World Medical, Inc.

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  • K231051 — Ahmed® Glaucoma Valve Model FP8 (May 12, 2023)
  • K230975 — Ahmed® Glaucoma Valve Model FP7 (May 12, 2023)
  • K211680 — Streamline Surgical System (October 8, 2021)
  • K182518 — AHMED ClearPath Glaucoma Drainage Device (January 18, 2019)
  • K171451 — Ahmed Glaucoma Valve Model FP8 (August 8, 2017)
  • K162060 — Ahmed Glaucoma Valve (October 24, 2016)
  • K060644 — AHMED GLAUCOMA VALVE, MODEL M4 (September 18, 2006)
  • K991072 — AHMED GLAUCOMA VALVE IMPLANT (July 13, 1999)
  • K980657 — AHMED GLAUCOMA VALVE, MODEL S3 (April 20, 1998)

Other clearances for product code MRH

  • K232214 — OMNI Surgical System (August 25, 2023)
  • K213173 — TrabEx Pro (June 8, 2022)
  • K212797 — iPrime Viscodelivery System (January 6, 2022)
  • K211680 — Streamline Surgical System (October 8, 2021)
  • K202678 — OMNI Surgical System (March 1, 2021)
  • K201953 — OMNI PLUS Surgical System (August 11, 2020)
  • K173332 — OMNI Surgical System (December 21, 2017)
  • K171905 — VISCO 360 Viscosurgical System (July 27, 2017)
  • K143205 — Viscoelastic Injector (December 5, 2014)
  • K132494 — VISCOELASTIC INJECTOR (October 22, 2013)