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FDA 510(k)

SMITH & NEPHEW DYONICS LEVELERT SYSTEM

K-Number: K903193 · 1990-08-30

ApplicantSmith & Nephew Dyonics, Inc.
Decision Date1990-08-30
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW DYONICS LEVELERT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Dyonics, Inc.. It received FDA 510(k) clearance on 1990-08-30 under 510(k) number K903193. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW DYONICS LEVELERT SYSTEM?

SMITH & NEPHEW DYONICS LEVELERT SYSTEM is a medical device that received FDA 510(k) clearance on 1990-08-30. The listed applicant is Smith & Nephew Dyonics, Inc.. The 510(k) number is K903193.

When did SMITH & NEPHEW DYONICS LEVELERT SYSTEM receive FDA 510(k) clearance?

SMITH & NEPHEW DYONICS LEVELERT SYSTEM received FDA 510(k) clearance on 1990-08-30, under 510(k) number K903193.

Who is the listed applicant for SMITH & NEPHEW DYONICS LEVELERT SYSTEM?

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

What is the FDA product code for SMITH & NEPHEW DYONICS LEVELERT SYSTEM?

The FDA product code for SMITH & NEPHEW DYONICS LEVELERT SYSTEM is FLN.

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Other records listing Smith & Nephew Dyonics, Inc. as applicant

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Related Devices (Code: FLN)

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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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