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FDA 510(k)

Alians Elbow Locking Plating System

K-Number: K171372 · 2018-01-04

ApplicantNewclip Technics
Decision Date2018-01-04
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Alians Elbow Locking Plating System is a medical device manufactured by Newclip Technics. It received FDA 510(k) clearance on 2018-01-04 under approval number K171372. 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 Alians Elbow Locking Plating System?

Alians Elbow Locking Plating System is a medical device that received FDA 510(k) clearance on 2018-01-04. It is manufactured by Newclip Technics. The 510(k) number is K171372.

When was Alians Elbow Locking Plating System approved by the FDA?

Alians Elbow Locking Plating System received FDA 510(k) clearance on 2018-01-04, under approval number K171372.

What company makes Alians Elbow Locking Plating System?

Alians Elbow Locking Plating System is manufactured by Newclip Technics.

What is the FDA product code for Alians Elbow Locking Plating System?

The FDA product code for Alians Elbow Locking Plating System is HRS.

Related Clinical Trials

NCT03487250 Percutaneous US Guided Elbow Tenotomy With the TenJet HydroSurgery System COMPLETED NCT07520851 Efficacy of the Buzzy System on Pain and Fear Reduction in Elbow Fracture Pin Removal RECRUITING NCT06772142 Early Feasibility of the Nervonik Peripheral Nerve Stimulation Device RECRUITING NCT07495254 Effectiveness of Combined Super Inductive System (SIS) Therapy With Therapeutic Exercise and Health Education in Lateral Elbow Tendinopathy NOT_YET_RECRUITING

Other Devices by Newclip Technics

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Related Devices (Code: HRS)

K163086VLP MINI-MOD 2.0mm Column PlatesSmith & Nephew, Inc. K162829Medline UNITE® Ankle Fracture Plating SystemMedline Industries, Inc. K162974Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation K163007Biomet Microfixation SternaLock 360 Sternal Closure SystemBiomet Microfixation K161696aap LOQTEQ® Distal Lateral Humerus Plate 2.7/3.5Aap Implantate AG K161747LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5Aap Implantate AG

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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