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FDA 510(k)

AOS Small Bone Nailing System

K-Number: K163014 · 2017-01-24

ApplicantAdvanced Orthopaedic Solutions, Inc. (Aos)
Decision Date2017-01-24
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AOS Small Bone Nailing System is a medical device manufactured by Advanced Orthopaedic Solutions, Inc. (Aos). It received FDA 510(k) clearance on 2017-01-24 under approval number K163014. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOS Small Bone Nailing System?

AOS Small Bone Nailing System is a medical device that received FDA 510(k) clearance on 2017-01-24. It is manufactured by Advanced Orthopaedic Solutions, Inc. (Aos). The 510(k) number is K163014.

When was AOS Small Bone Nailing System approved by the FDA?

AOS Small Bone Nailing System received FDA 510(k) clearance on 2017-01-24, under approval number K163014.

What company makes AOS Small Bone Nailing System?

AOS Small Bone Nailing System is manufactured by Advanced Orthopaedic Solutions, Inc. (Aos).

What is the FDA product code for AOS Small Bone Nailing System?

The FDA product code for AOS Small Bone Nailing System is HSB.

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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)

K161913AOS Small Fragment Plating System K171606AOS Anterolateral Proximal Humeral Plate K181035AOS Small Fragment Plating System Lite

Related Devices (Code: HSB)

K161264TRIGEN Low Profile Bone ScrewsSmith & Nephew, Inc. K160545GAP ENDO-EXO MEDULLARY SYSTEMPega Medical, Inc. K161254Renovo Life Small Bone IM Nail SystemRenovo Life, LLC K160167DePuy Synthes TFNA Augmentation SystemSynthes (USA) Products, LLC K160325PRECICE Intramedullary Limb Lengthening SystemEllipse Technologies, Inc. K160267PRECICE Trauma Nail SystemEllipse Technologies, Incorporated

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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