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FDA 510(k)

MESH GPS - LARGE, SMALL, SM, SM SMALL

K-Number: K092726 · 2010-03-15

ApplicantSurgical Structures , Ltd.
Decision Date2010-03-15
Product CodeOQL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MESH GPS - LARGE, SMALL, SM, SM SMALL is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Structures , Ltd.. It received FDA 510(k) clearance on 2010-03-15 under 510(k) number K092726. The device is classified under product code OQL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MESH GPS - LARGE, SMALL, SM, SM SMALL?

MESH GPS - LARGE, SMALL, SM, SM SMALL is a medical device that received FDA 510(k) clearance on 2010-03-15. The listed applicant is Surgical Structures , Ltd.. The 510(k) number is K092726.

When did MESH GPS - LARGE, SMALL, SM, SM SMALL receive FDA 510(k) clearance?

MESH GPS - LARGE, SMALL, SM, SM SMALL received FDA 510(k) clearance on 2010-03-15, under 510(k) number K092726.

Who is the listed applicant for MESH GPS - LARGE, SMALL, SM, SM SMALL?

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

What is the FDA product code for MESH GPS - LARGE, SMALL, SM, SM SMALL?

The FDA product code for MESH GPS - LARGE, SMALL, SM, SM SMALL is OQL.

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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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