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FDA 510(k)

Piccolo Composite Nailing System

K-Number: K173652 · 2017-12-28

Decision Date2017-12-28
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Piccolo Composite Nailing System is a medical device manufactured by CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2017-12-28 under approval number K173652. 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 Piccolo Composite Nailing System?

Piccolo Composite Nailing System is a medical device that received FDA 510(k) clearance on 2017-12-28. It is manufactured by CarboFix Orthopedics , Ltd.. The 510(k) number is K173652.

When was Piccolo Composite Nailing System approved by the FDA?

Piccolo Composite Nailing System received FDA 510(k) clearance on 2017-12-28, under approval number K173652.

What company makes Piccolo Composite Nailing System?

Piccolo Composite Nailing System is manufactured by CarboFix Orthopedics , Ltd..

What is the FDA product code for Piccolo Composite Nailing System?

The FDA product code for Piccolo Composite Nailing System is HSB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.