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FDA 510(k)

ProRib Fixation System

K-Number: K261892 · 2026-09-23

Decision Date2026-09-23
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ProRib Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Costa Surgical, Inc.. It received FDA 510(k) clearance on 2026-09-23 under 510(k) number K261892. 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 ProRib Fixation System?

ProRib Fixation System is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Costa Surgical, Inc.. The 510(k) number is K261892.

When did ProRib Fixation System receive FDA 510(k) clearance?

ProRib Fixation System received FDA 510(k) clearance on 2026-09-23, under 510(k) number K261892.

Who is the listed applicant for ProRib Fixation System?

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

What is the FDA product code for ProRib Fixation System?

The FDA product code for ProRib Fixation System is HRS.

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.

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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