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FDA 510(k)

STRYKER MMF SCREW

K-Number: K050535 · 2005-03-17

ApplicantStryker Instruments
Decision Date2005-03-17
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRYKER MMF SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2005-03-17 under 510(k) number K050535. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER MMF SCREW?

STRYKER MMF SCREW is a medical device that received FDA 510(k) clearance on 2005-03-17. The listed applicant is Stryker Instruments. The 510(k) number is K050535.

When did STRYKER MMF SCREW receive FDA 510(k) clearance?

STRYKER MMF SCREW received FDA 510(k) clearance on 2005-03-17, under 510(k) number K050535.

Who is the listed applicant for STRYKER MMF SCREW?

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

What is the FDA product code for STRYKER MMF SCREW?

The FDA product code for STRYKER MMF SCREW is DZL.

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Related Devices (Code: DZL)

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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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