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FDA 510(k)

SURGICRAFT SURGICAL MESH SYSTEM

K-Number: K072370 · 2008-07-24

ApplicantSurgicraft , Ltd.
Decision Date2008-07-24
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICRAFT SURGICAL MESH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgicraft , Ltd.. It received FDA 510(k) clearance on 2008-07-24 under 510(k) number K072370. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICRAFT SURGICAL MESH SYSTEM?

SURGICRAFT SURGICAL MESH SYSTEM is a medical device that received FDA 510(k) clearance on 2008-07-24. The listed applicant is Surgicraft , Ltd.. The 510(k) number is K072370.

When did SURGICRAFT SURGICAL MESH SYSTEM receive FDA 510(k) clearance?

SURGICRAFT SURGICAL MESH SYSTEM received FDA 510(k) clearance on 2008-07-24, under 510(k) number K072370.

Who is the listed applicant for SURGICRAFT SURGICAL MESH SYSTEM?

The FDA 510(k) record lists Surgicraft , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICRAFT SURGICAL MESH SYSTEM?

The FDA product code for SURGICRAFT SURGICAL MESH SYSTEM is FTL.

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Other records listing Surgicraft , Ltd. as applicant

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Related Devices (Code: FTL)

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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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