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FDA 510(k)

Connector System

K-Number: K170647 · 2017-05-11

ApplicantOrthofix, Inc.
Decision Date2017-05-11
Product CodeNKG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Connector System is the device name listed in this FDA 510(k) record. The listed applicant is Orthofix, Inc.. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K170647. 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 2017-05-11. The listed applicant is Orthofix, Inc.. The 510(k) number is K170647.

When did Connector System receive FDA 510(k) clearance?

Connector System received FDA 510(k) clearance on 2017-05-11, under 510(k) number K170647.

Who is the listed applicant for Connector System?

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

What is the FDA product code for Connector System?

The FDA product code for Connector System is NKG.

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Related Devices (Code: NKG)

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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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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