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FDA 510(k)

TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER

K-Number: K032238 · 2003-09-09

ApplicantNeurosel (Medical) Limited
Decision Date2003-09-09
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Neurosel (Medical) Limited. It received FDA 510(k) clearance on 2003-09-09 under 510(k) number K032238. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER?

TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER is a medical device that received FDA 510(k) clearance on 2003-09-09. The listed applicant is Neurosel (Medical) Limited. The 510(k) number is K032238.

When did TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER receive FDA 510(k) clearance?

TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER received FDA 510(k) clearance on 2003-09-09, under 510(k) number K032238.

Who is the listed applicant for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER?

The FDA 510(k) record lists Neurosel (Medical) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER?

The FDA product code for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER is FZP.

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Related Devices (Code: FZP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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