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FDA 510(k)

STRYKER POWER TOOL NAVIGATOR ATTACHMENT

K-Number: K080450 · 2008-07-17

ApplicantStryker Corp.
Decision Date2008-07-17
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER POWER TOOL NAVIGATOR ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2008-07-17 under 510(k) number K080450. 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 POWER TOOL NAVIGATOR ATTACHMENT?

STRYKER POWER TOOL NAVIGATOR ATTACHMENT is a medical device that received FDA 510(k) clearance on 2008-07-17. The listed applicant is Stryker Corp.. The 510(k) number is K080450.

When did STRYKER POWER TOOL NAVIGATOR ATTACHMENT receive FDA 510(k) clearance?

STRYKER POWER TOOL NAVIGATOR ATTACHMENT received FDA 510(k) clearance on 2008-07-17, under 510(k) number K080450.

Who is the listed applicant for STRYKER POWER TOOL NAVIGATOR ATTACHMENT?

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 POWER TOOL NAVIGATOR ATTACHMENT?

The FDA product code for STRYKER POWER TOOL NAVIGATOR ATTACHMENT is HAW.

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Other records listing Stryker Corp. as applicant

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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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