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FDA 510(k)

LOQTEQ VA Foot Plates 2.5

K-Number: K182785 · 2019-06-19

ApplicantAap Implantate AG
Decision Date2019-06-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LOQTEQ VA Foot Plates 2.5 is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2019-06-19 under 510(k) number K182785. 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 LOQTEQ VA Foot Plates 2.5?

LOQTEQ VA Foot Plates 2.5 is a medical device that received FDA 510(k) clearance on 2019-06-19. The listed applicant is Aap Implantate AG. The 510(k) number is K182785.

When did LOQTEQ VA Foot Plates 2.5 receive FDA 510(k) clearance?

LOQTEQ VA Foot Plates 2.5 received FDA 510(k) clearance on 2019-06-19, under 510(k) number K182785.

Who is the listed applicant for LOQTEQ VA Foot Plates 2.5?

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

What is the FDA product code for LOQTEQ VA Foot Plates 2.5?

The FDA product code for LOQTEQ VA Foot Plates 2.5 is HRS.

Other records listing Aap Implantate AG 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.

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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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