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FDA 510(k)

DePuy Synthes 2.7mm VA LCP Clavicle Plate System

K-Number: K201321 · 2020-07-24

ApplicantDePuy Synthes
Decision Date2020-07-24
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy Synthes 2.7mm VA LCP Clavicle Plate System is a medical device manufactured by DePuy Synthes. It received FDA 510(k) clearance on 2020-07-24 under approval number K201321. 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 DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

DePuy Synthes 2.7mm VA LCP Clavicle Plate System is a medical device that received FDA 510(k) clearance on 2020-07-24. It is manufactured by DePuy Synthes. The 510(k) number is K201321.

When was DePuy Synthes 2.7mm VA LCP Clavicle Plate System approved by the FDA?

DePuy Synthes 2.7mm VA LCP Clavicle Plate System received FDA 510(k) clearance on 2020-07-24, under approval number K201321.

What company makes DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

DePuy Synthes 2.7mm VA LCP Clavicle Plate System is manufactured by DePuy Synthes.

What is the FDA product code for DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

The FDA product code for DePuy Synthes 2.7mm VA LCP Clavicle Plate System is HRS.

Related Clinical Trials

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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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