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FDA 510(k)

FAST THROW STAINLESS STEEL SURGICAL SUTURE

K-Number: K030926 · 2003-07-21

Decision Date2003-07-21
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FAST THROW STAINLESS STEEL SURGICAL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Products, Inc.. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K030926. 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 FAST THROW STAINLESS STEEL SURGICAL SUTURE?

FAST THROW STAINLESS STEEL SURGICAL SUTURE is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is Advanced Surgical Products, Inc.. The 510(k) number is K030926.

When did FAST THROW STAINLESS STEEL SURGICAL SUTURE receive FDA 510(k) clearance?

FAST THROW STAINLESS STEEL SURGICAL SUTURE received FDA 510(k) clearance on 2003-07-21, under 510(k) number K030926.

Who is the listed applicant for FAST THROW STAINLESS STEEL SURGICAL SUTURE?

The FDA 510(k) record lists Advanced Surgical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FAST THROW STAINLESS STEEL SURGICAL SUTURE?

The FDA product code for FAST THROW STAINLESS STEEL SURGICAL SUTURE is FZP.

Related Clinical Trials

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.

Other records listing Advanced Surgical Products, Inc. as applicant

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.

View all 64 devices →

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.

Official Source

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

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