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510(k) K232373

Progrip™ Self-Gripping Polypropylene Mesh by Sofradim Production — Product Code FTL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 18, 2024
Date Received
August 8, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical, Polymeric
Device Class
Class II
Regulation Number
878.3300
Review Panel
SU
Submission Type

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  • K223218 — Parietene Macroporous Mesh (December 2, 2022)
  • K220586 — Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh, Parietex Hydrophi (June 22, 2022)
  • K192443 — Dextile Anatomical Mesh (December 6, 2019)
  • K173796 — Parietex Surgical Mesh (modified into Parietex Hydrophilic 2D, 3D, Anatomical Me (March 9, 2018)
  • K172395 — Duatene bilayer mesh (February 1, 2018)
  • K163212 — Parietene DS Composite Mesh (June 29, 2017)
  • K150091 — Versatex Monofilament Mesh (May 26, 2015)

Other clearances for product code FTL

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  • K250869 — Parietene™ Macroporous Mesh (PPM5050 ) (April 23, 2025)
  • K250098 — Bard Soft Mesh; Bard Soft Mesh Pre-Shaped (April 9, 2025)
  • K243315 — ProGrip™ Self-Gripping Polypropylene Mesh (January 17, 2025)
  • K241250 — 3DMax Light Mesh (June 14, 2024)
  • K233402 — Bard 3DMax Mesh (November 1, 2023)
  • K232924 — T-Line® Hernia Mesh (October 18, 2023)
  • K230671 — Pitch PaSoft Tissue Reinforcement Device (May 31, 2023)