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FDA 510(k)

AOS Small Fragment Plating System

K-Number: K161913 · 2016-11-04

ApplicantAdvanced Orthopaedic Solutions, Inc. (Aos)
Decision Date2016-11-04
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AOS Small Fragment Plating System is a medical device manufactured by Advanced Orthopaedic Solutions, Inc. (Aos). It received FDA 510(k) clearance on 2016-11-04 under approval number K161913. 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 AOS Small Fragment Plating System?

AOS Small Fragment Plating System is a medical device that received FDA 510(k) clearance on 2016-11-04. It is manufactured by Advanced Orthopaedic Solutions, Inc. (Aos). The 510(k) number is K161913.

When was AOS Small Fragment Plating System approved by the FDA?

AOS Small Fragment Plating System received FDA 510(k) clearance on 2016-11-04, under approval number K161913.

What company makes AOS Small Fragment Plating System?

AOS Small Fragment Plating System is manufactured by Advanced Orthopaedic Solutions, Inc. (Aos).

What is the FDA product code for AOS Small Fragment Plating System?

The FDA product code for AOS Small Fragment Plating System is HRS.

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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)

Other Devices by Advanced Orthopaedic Solutions, Inc. (Aos)

K171606AOS Anterolateral Proximal Humeral Plate K163014AOS Small Bone Nailing System K181035AOS Small Fragment Plating System Lite

Related Devices (Code: HRS)

K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc. K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc. K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG

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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