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FDA 510(k)

DePuy PINNACLE Dual Mobility Liner

K-Number: K200854 · 2020-09-11

ApplicantDepuy Ireland UC
Decision Date2020-09-11
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DePuy PINNACLE Dual Mobility Liner is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Ireland UC. It received FDA 510(k) clearance on 2020-09-11 under 510(k) number K200854. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DePuy PINNACLE Dual Mobility Liner?

DePuy PINNACLE Dual Mobility Liner is a medical device that received FDA 510(k) clearance on 2020-09-11. The listed applicant is Depuy Ireland UC. The 510(k) number is K200854.

When did DePuy PINNACLE Dual Mobility Liner receive FDA 510(k) clearance?

DePuy PINNACLE Dual Mobility Liner received FDA 510(k) clearance on 2020-09-11, under 510(k) number K200854.

Who is the listed applicant for DePuy PINNACLE Dual Mobility Liner?

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

What is the FDA product code for DePuy PINNACLE Dual Mobility Liner?

The FDA product code for DePuy PINNACLE Dual Mobility Liner is LPH.

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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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