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FDA 510(k)

MobiliT Cup

K-Number: K191831 · 2020-01-16

ApplicantCorin U.S.A. Limited
Decision Date2020-01-16
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MobiliT Cup is the device name listed in this FDA 510(k) record. The listed applicant is Corin U.S.A. Limited. It received FDA 510(k) clearance on 2020-01-16 under 510(k) number K191831. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MobiliT Cup?

MobiliT Cup is a medical device that received FDA 510(k) clearance on 2020-01-16. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K191831.

When did MobiliT Cup receive FDA 510(k) clearance?

MobiliT Cup received FDA 510(k) clearance on 2020-01-16, under 510(k) number K191831.

Who is the listed applicant for MobiliT Cup?

The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MobiliT Cup?

The FDA product code for MobiliT Cup is LZO.

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Related Devices (Code: LZO)

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.

K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbHK252401implaFit® short stemsImplantcast GmbHK253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)Maxx Orthopedics, Inc.

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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