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FDA 510(k)

STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE

K-Number: K072271 · 2007-12-18

ApplicantStryker Corp.
Decision Date2007-12-18
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING 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 2007-12-18 under 510(k) number K072271. 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 INFINITUS HIP RESURFACING MODULE?

STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE is a medical device that received FDA 510(k) clearance on 2007-12-18. The listed applicant is Stryker Corp.. The 510(k) number is K072271.

When did STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE receive FDA 510(k) clearance?

STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE received FDA 510(k) clearance on 2007-12-18, under 510(k) number K072271.

Who is the listed applicant for STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING 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 INFINITUS HIP RESURFACING MODULE?

The FDA product code for STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE is HAW.

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Other records listing Stryker Corp. 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.

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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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