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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 the device name listed in this FDA 510(k) record. The listed applicant is CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2017-12-28 under 510(k) 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. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K173652.

When did Piccolo Composite Nailing System receive FDA 510(k) clearance?

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

Who is the listed applicant for Piccolo Composite Nailing System?

The FDA 510(k) record lists CarboFix Orthopedics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing CarboFix Orthopedics , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: HSB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.