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FDA 510(k)

Connector System

K-Number: K172194 · 2017-08-18

ApplicantOrthofix, Inc.
Decision Date2017-08-18
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Connector System is a medical device manufactured by Orthofix, Inc.. It received FDA 510(k) clearance on 2017-08-18 under approval number K172194. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Connector System?

Connector System is a medical device that received FDA 510(k) clearance on 2017-08-18. It is manufactured by Orthofix, Inc.. The 510(k) number is K172194.

When was Connector System approved by the FDA?

Connector System received FDA 510(k) clearance on 2017-08-18, under approval number K172194.

What company makes Connector System?

Connector System is manufactured by Orthofix, Inc..

What is the FDA product code for Connector System?

The FDA product code for Connector System is NKG.

Other Devices by Orthofix, Inc.

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Related Devices (Code: NKG)

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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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