HIP MODULE FOR THE STEALTHSTATION SYSTEM
K-Number: K021980 · 2002-11-19
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Device Summary
Frequently Asked Questions
What is the HIP MODULE FOR THE STEALTHSTATION SYSTEM?
HIP MODULE FOR THE STEALTHSTATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Medtronic Surgical Navigation Technologies. The 510(k) number is K021980.
When did HIP MODULE FOR THE STEALTHSTATION SYSTEM receive FDA 510(k) clearance?
HIP MODULE FOR THE STEALTHSTATION SYSTEM received FDA 510(k) clearance on 2002-11-19, under 510(k) number K021980.
Who is the listed applicant for HIP MODULE FOR THE STEALTHSTATION SYSTEM?
The FDA 510(k) record lists Medtronic Surgical Navigation Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIP MODULE FOR THE STEALTHSTATION SYSTEM?
The FDA product code for HIP 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 Medtronic Surgical Navigation Technologies 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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