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FDA 510(k)

FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM

K-Number: K990214 · 1999-04-22

Decision Date1999-04-22
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Navigation Technologies, Inc.. It received FDA 510(k) clearance on 1999-04-22 under 510(k) number K990214. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM?

FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1999-04-22. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K990214.

When did FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM receive FDA 510(k) clearance?

FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM received FDA 510(k) clearance on 1999-04-22, under 510(k) number K990214.

Who is the listed applicant for FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM?

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

What is the FDA product code for FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM?

The FDA product code for FLUORONAV MODULE FOR THE STEALTHSTATION SYSTEM is HAW.

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 Surgical Navigation Technologies, 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 27 devices →

Related Devices (Code: HAW)

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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