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FDA 510(k)

Activmotion S DTO

K-Number: K202803 · 2021-12-16

ApplicantNewclip Technics
Decision Date2021-12-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Activmotion S DTO is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2021-12-16 under 510(k) number K202803. 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 Activmotion S DTO?

Activmotion S DTO is a medical device that received FDA 510(k) clearance on 2021-12-16. The listed applicant is Newclip Technics. The 510(k) number is K202803.

When did Activmotion S DTO receive FDA 510(k) clearance?

Activmotion S DTO received FDA 510(k) clearance on 2021-12-16, under 510(k) number K202803.

Who is the listed applicant for Activmotion S DTO?

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

What is the FDA product code for Activmotion S DTO?

The FDA product code for Activmotion S DTO is HRS.

Other records listing Newclip Technics 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.

K261511Xpert AnkleK261191Alians Elbow SK261038Xpert PFPK253906Xpert HandK250767Newclip Patient-matched instrumentation non sterile PSIK250155Xpert Knee

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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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