FDA 510(k)

SIMMONS PLATING SYSTEM BOLT AND SCREW

K-Number: K930353 · 1995-06-20

Decision Date1995-06-20

Product CodeMNH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SIMMONS PLATING SYSTEM BOLT AND SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1995-06-20 under 510(k) number K930353. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMMONS PLATING SYSTEM BOLT AND SCREW?

SIMMONS PLATING SYSTEM BOLT AND SCREW is a medical device that received FDA 510(k) clearance on 1995-06-20. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K930353.

When did SIMMONS PLATING SYSTEM BOLT AND SCREW receive FDA 510(k) clearance?

SIMMONS PLATING SYSTEM BOLT AND SCREW received FDA 510(k) clearance on 1995-06-20, under 510(k) number K930353.

Who is the listed applicant for SIMMONS PLATING SYSTEM BOLT AND SCREW?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMMONS PLATING SYSTEM BOLT AND SCREW?

The FDA product code for SIMMONS PLATING SYSTEM BOLT AND SCREW is MNH. This falls under the ENT category.

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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.