STEALTHSTATION SYSTEM DIGITIZER CHANGE
K-Number: K981686 · 1998-08-07
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Device Summary
Frequently Asked Questions
What is the STEALTHSTATION SYSTEM DIGITIZER CHANGE?
STEALTHSTATION SYSTEM DIGITIZER CHANGE is a medical device that received FDA 510(k) clearance on 1998-08-07. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K981686.
When did STEALTHSTATION SYSTEM DIGITIZER CHANGE receive FDA 510(k) clearance?
STEALTHSTATION SYSTEM DIGITIZER CHANGE received FDA 510(k) clearance on 1998-08-07, under 510(k) number K981686.
Who is the listed applicant for STEALTHSTATION SYSTEM DIGITIZER CHANGE?
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 SYSTEM DIGITIZER CHANGE?
The FDA product code for STEALTHSTATION SYSTEM DIGITIZER CHANGE 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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