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FDA 510(k)

STRYKER INJECTABLE CEMENT

K-Number: K051603 · 2005-12-30

ApplicantStryker Leibinger Micro Implants
Decision Date2005-12-30
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER INJECTABLE CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger Micro Implants. It received FDA 510(k) clearance on 2005-12-30 under 510(k) number K051603. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER INJECTABLE CEMENT?

STRYKER INJECTABLE CEMENT is a medical device that received FDA 510(k) clearance on 2005-12-30. The listed applicant is Stryker Leibinger Micro Implants. The 510(k) number is K051603.

When did STRYKER INJECTABLE CEMENT receive FDA 510(k) clearance?

STRYKER INJECTABLE CEMENT received FDA 510(k) clearance on 2005-12-30, under 510(k) number K051603.

Who is the listed applicant for STRYKER INJECTABLE CEMENT?

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

What is the FDA product code for STRYKER INJECTABLE CEMENT?

The FDA product code for STRYKER INJECTABLE CEMENT is MQV.

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Other records listing Stryker Leibinger Micro Implants 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.

K213777Stryker Resorbable Fixation System

Related Devices (Code: MQV)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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