Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

METHA SHORT STEM HIP SYSTEM

K-Number: K080584 · 2008-05-09

Decision Date2008-05-09
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

METHA SHORT STEM HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Implant System, Inc.. It received FDA 510(k) clearance on 2008-05-09 under 510(k) number K080584. 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 METHA SHORT STEM HIP SYSTEM?

METHA SHORT STEM HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2008-05-09. The listed applicant is Aesculap Implant System, Inc.. The 510(k) number is K080584.

When did METHA SHORT STEM HIP SYSTEM receive FDA 510(k) clearance?

METHA SHORT STEM HIP SYSTEM received FDA 510(k) clearance on 2008-05-09, under 510(k) number K080584.

Who is the listed applicant for METHA SHORT STEM HIP SYSTEM?

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

What is the FDA product code for METHA SHORT STEM HIP SYSTEM?

The FDA product code for METHA SHORT STEM HIP SYSTEM is MEH.

Related Clinical Trials

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.

Other records listing Aesculap Implant System, Inc. as applicant

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.

View all 15 devices →

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.

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.

↑