TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER— 510(k) K032238

Name: FDA 510(k) clearance K032238
Creator: U.S. Food and Drug Administration
Published: 2003-09-09

Substantially Equivalent

Neurosel (Medical) Limited

FDA 510(k) clearance K032238 for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER, Substantially Equivalent on 2003-09-09. Applicant: Neurosel (Medical) Limited. Device class: 2.

Clearance details

Applicant: Neurosel (Medical) Limited
Product code: Code FZP
Device class: Class 2
Regulation: 21 CFR 878.4300
Advisory panel: General, Plastic Surgery
Date received: 2003-07-21
Decision date: 2003-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, Hampshire, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZP

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K253781 — InnoClip Clip Applier2025-12-22
K253903 — InnoClip Disposable Clip Applier2025-12-22
K250643 — Disposable Polymer Ligation Clips2025-11-20
K251054 — Hem-o-lok PurplePlus Large Polymer Ligating Clips2025-07-03

Adverse events under product code FZP

product code FZP

Death: 11
Injury: 726
Malfunction: 10,830
Other: 1
Total: 11,568

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.