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FDA 510(k)

AdvantageRib Anterior System

K-Number: K182179 · 2018-11-16

ApplicantSig Medical Corp.
Decision Date2018-11-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AdvantageRib Anterior System is the device name listed in this FDA 510(k) record. The listed applicant is Sig Medical Corp.. It received FDA 510(k) clearance on 2018-11-16 under 510(k) number K182179. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AdvantageRib Anterior System?

AdvantageRib Anterior System is a medical device that received FDA 510(k) clearance on 2018-11-16. The listed applicant is Sig Medical Corp.. The 510(k) number is K182179.

When did AdvantageRib Anterior System receive FDA 510(k) clearance?

AdvantageRib Anterior System received FDA 510(k) clearance on 2018-11-16, under 510(k) number K182179.

Who is the listed applicant for AdvantageRib Anterior System?

The FDA 510(k) record lists Sig Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AdvantageRib Anterior System?

The FDA product code for AdvantageRib Anterior System is HRS.

Other records listing Sig Medical Corp. 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.

K183317AdvantageRib System

Related Devices (Code: HRS)

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

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

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