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FDA 510(k)

STRYKER NAVIGATION SYSTEM - ENT MODULE

K-Number: K002732 · 2000-10-02

ApplicantStryker Corp.
Decision Date2000-10-02
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER NAVIGATION SYSTEM - ENT MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2000-10-02 under 510(k) number K002732. 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 STRYKER NAVIGATION SYSTEM - ENT MODULE?

STRYKER NAVIGATION SYSTEM - ENT MODULE is a medical device that received FDA 510(k) clearance on 2000-10-02. The listed applicant is Stryker Corp.. The 510(k) number is K002732.

When did STRYKER NAVIGATION SYSTEM - ENT MODULE receive FDA 510(k) clearance?

STRYKER NAVIGATION SYSTEM - ENT MODULE received FDA 510(k) clearance on 2000-10-02, under 510(k) number K002732.

Who is the listed applicant for STRYKER NAVIGATION SYSTEM - ENT MODULE?

The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER NAVIGATION SYSTEM - ENT MODULE?

The FDA product code for STRYKER NAVIGATION SYSTEM - ENT MODULE is HAW.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: HAW)

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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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