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FDA 510(k)

VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE

K-Number: K991706 · 1999-12-07

ApplicantStryker Corp.
Decision Date1999-12-07
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1999-12-07 under 510(k) number K991706. 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 VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE?

VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE is a medical device that received FDA 510(k) clearance on 1999-12-07. The listed applicant is Stryker Corp.. The 510(k) number is K991706.

When did VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE receive FDA 510(k) clearance?

VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE received FDA 510(k) clearance on 1999-12-07, under 510(k) number K991706.

Who is the listed applicant for VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE?

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 VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE?

The FDA product code for VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE 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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