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FDA 510(k)

SECURE-LOCK

K-Number: K220906 · 2022-07-22

ApplicantXiros, Ltd.
Decision Date2022-07-22
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SECURE-LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Xiros, Ltd.. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220906. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECURE-LOCK?

SECURE-LOCK is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Xiros, Ltd.. The 510(k) number is K220906.

When did SECURE-LOCK receive FDA 510(k) clearance?

SECURE-LOCK received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220906.

Who is the listed applicant for SECURE-LOCK?

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

What is the FDA product code for SECURE-LOCK?

The FDA product code for SECURE-LOCK is HTY.

Related Clinical Trials

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Other records listing Xiros, Ltd. as applicant

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K242237Jewel Soft Tissue Reinforcement Device (102-6005)K230671Pitch PaSoft Tissue Reinforcement DeviceK222978Poly-Tape/Infinity-Lock Soft Tissue Reinforcement DeviceK220091Poly-Tape/Infinity-Lock Soft Tissue Reinforcement DeviceK211563Pitch-PatchsK191053Xtreme-Loop

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Related Devices (Code: HTY)

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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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