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FDA 510(k)

HIP MODULE FOR THE STEALTHSTATION SYSTEM

K-Number: K021980 · 2002-11-19

Decision Date2002-11-19
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HIP MODULE FOR THE STEALTHSTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Surgical Navigation Technologies. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K021980. 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 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.

View all 12 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

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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