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FDA 510(k)

PREVISION HIP SYSTEM WITH RECON RING

K-Number: K102424 · 2010-12-09

ApplicantAesculap Implant Systems, LLC
Decision Date2010-12-09
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PREVISION HIP SYSTEM WITH RECON RING is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Implant Systems, LLC. It received FDA 510(k) clearance on 2010-12-09 under 510(k) number K102424. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREVISION HIP SYSTEM WITH RECON RING?

PREVISION HIP SYSTEM WITH RECON RING is a medical device that received FDA 510(k) clearance on 2010-12-09. The listed applicant is Aesculap Implant Systems, LLC. The 510(k) number is K102424.

When did PREVISION HIP SYSTEM WITH RECON RING receive FDA 510(k) clearance?

PREVISION HIP SYSTEM WITH RECON RING received FDA 510(k) clearance on 2010-12-09, under 510(k) number K102424.

Who is the listed applicant for PREVISION HIP SYSTEM WITH RECON RING?

The FDA 510(k) record lists Aesculap Implant Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PREVISION HIP SYSTEM WITH RECON RING?

The FDA product code for PREVISION HIP SYSTEM WITH RECON RING is MEH.

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Other records listing Aesculap Implant Systems, LLC as applicant

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Related Devices (Code: MEH)

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.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, 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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