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FDA 510(k)

Anteralign LS coverplate

K-Number: K260810 · 2026-06-10

ApplicantTyber Medical, LLC
Decision Date2026-06-10
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Anteralign LS coverplate is the device name listed in this FDA 510(k) record. The listed applicant is Tyber Medical, LLC. It received FDA 510(k) clearance on 2026-06-10 under 510(k) number K260810. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Anteralign LS coverplate?

Anteralign LS coverplate is a medical device that received FDA 510(k) clearance on 2026-06-10. The listed applicant is Tyber Medical, LLC. The 510(k) number is K260810.

When did Anteralign LS coverplate receive FDA 510(k) clearance?

Anteralign LS coverplate received FDA 510(k) clearance on 2026-06-10, under 510(k) number K260810.

Who is the listed applicant for Anteralign LS coverplate?

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

What is the FDA product code for Anteralign LS coverplate?

The FDA product code for Anteralign LS coverplate is OVD.

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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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