STEALTHSTATION TREATMENT GUIDANCE PLATFORM
K-Number: K981768 · 1998-11-23
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Device Summary
Frequently Asked Questions
What is the STEALTHSTATION TREATMENT GUIDANCE PLATFORM?
STEALTHSTATION TREATMENT GUIDANCE PLATFORM is a medical device that received FDA 510(k) clearance on 1998-11-23. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K981768.
When did STEALTHSTATION TREATMENT GUIDANCE PLATFORM receive FDA 510(k) clearance?
STEALTHSTATION TREATMENT GUIDANCE PLATFORM received FDA 510(k) clearance on 1998-11-23, under 510(k) number K981768.
Who is the listed applicant for STEALTHSTATION TREATMENT GUIDANCE PLATFORM?
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 STEALTHSTATION TREATMENT GUIDANCE PLATFORM?
The FDA product code for STEALTHSTATION TREATMENT GUIDANCE PLATFORM 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.
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
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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