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FDA 510(k)

ABG II MONOLITHIC HIP STEM

K-Number: K110807 · 2011-05-25

ApplicantStryker Corp.
Decision Date2011-05-25
Product CodeMAY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ABG II MONOLITHIC HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2011-05-25 under 510(k) number K110807. The device is classified under product code MAY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABG II MONOLITHIC HIP STEM?

ABG II MONOLITHIC HIP STEM is a medical device that received FDA 510(k) clearance on 2011-05-25. The listed applicant is Stryker Corp.. The 510(k) number is K110807.

When did ABG II MONOLITHIC HIP STEM receive FDA 510(k) clearance?

ABG II MONOLITHIC HIP STEM received FDA 510(k) clearance on 2011-05-25, under 510(k) number K110807.

Who is the listed applicant for ABG II MONOLITHIC HIP STEM?

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 ABG II MONOLITHIC HIP STEM?

The FDA product code for ABG II MONOLITHIC HIP STEM is MAY.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: MAY)

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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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