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FDA 510(k)

STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM

K-Number: K984000 · 1999-01-12

Decision Date1999-01-12
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STEALTHSERVER IMAGE STORAGE AND COMMUNICATION 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 1999-01-12 under 510(k) number K984000. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM?

STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM is a medical device that received FDA 510(k) clearance on 1999-01-12. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K984000.

When did STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM receive FDA 510(k) clearance?

STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM received FDA 510(k) clearance on 1999-01-12, under 510(k) number K984000.

Who is the listed applicant for STEALTHSERVER IMAGE STORAGE AND COMMUNICATION 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 STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM?

The FDA product code for STEALTHSERVER IMAGE STORAGE AND COMMUNICATION SYSTEM is LMD.

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: LMD)

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

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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