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FDA 510(k)

A.L.P.S. Small Fragment Plating System

K-Number: K243761 · 2025-02-19

ApplicantBiomet Orthopedics
Decision Date2025-02-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A.L.P.S. Small Fragment Plating System is a medical device manufactured by Biomet Orthopedics. It received FDA 510(k) clearance on 2025-02-19 under approval number K243761. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.L.P.S. Small Fragment Plating System?

A.L.P.S. Small Fragment Plating System is a medical device that received FDA 510(k) clearance on 2025-02-19. It is manufactured by Biomet Orthopedics. The 510(k) number is K243761.

When was A.L.P.S. Small Fragment Plating System approved by the FDA?

A.L.P.S. Small Fragment Plating System received FDA 510(k) clearance on 2025-02-19, under approval number K243761.

What company makes A.L.P.S. Small Fragment Plating System?

A.L.P.S. Small Fragment Plating System is manufactured by Biomet Orthopedics.

What is the FDA product code for A.L.P.S. Small Fragment Plating System?

The FDA product code for A.L.P.S. Small Fragment Plating System is HRS.

Related Clinical Trials

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Related PubMed Literature

PMID: 42168293 Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling. Scientific reports (2026)

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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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