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FDA 510(k)

Pectus Support Bar System

K-Number: K213712 · 2022-03-11

ApplicantBiomet Microfixation
Decision Date2022-03-11
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Pectus Support Bar System is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Microfixation. It received FDA 510(k) clearance on 2022-03-11 under 510(k) number K213712. 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 Pectus Support Bar System?

Pectus Support Bar System is a medical device that received FDA 510(k) clearance on 2022-03-11. The listed applicant is Biomet Microfixation. The 510(k) number is K213712.

When did Pectus Support Bar System receive FDA 510(k) clearance?

Pectus Support Bar System received FDA 510(k) clearance on 2022-03-11, under 510(k) number K213712.

Who is the listed applicant for Pectus Support Bar System?

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

What is the FDA product code for Pectus Support Bar System?

The FDA product code for Pectus Support Bar System is HRS.

Other records listing Biomet Microfixation as applicant

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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.

K260277MIKRON TRAUMA BONE PLATE& SCREW SYSTEMMikron Makina San. ve Tic. Ltd. Sti.K261511Xpert AnkleNewclip TechnicsK261406Versalock Proximal Tibial Plating SystemGM Dos Reis Industria e Comercio Ltda.K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB )TriMed, Inc.K261191Alians Elbow SNewclip TechnicsK261054RibPlate SystemStryker Leibinger GmbH & Co KG

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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