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)

CEMENTLESS HIP PROSTHESIS

K-Number: K840271 · 1984-07-03

Decision Date1984-07-03
Product Code
DecisionSubstantially Equivalent

Device Summary

CEMENTLESS HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Mecron Medical Products, Inc.. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K840271. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENTLESS HIP PROSTHESIS?

CEMENTLESS HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Mecron Medical Products, Inc.. The 510(k) number is K840271.

When did CEMENTLESS HIP PROSTHESIS receive FDA 510(k) clearance?

CEMENTLESS HIP PROSTHESIS received FDA 510(k) clearance on 1984-07-03, under 510(k) number K840271.

Who is the listed applicant for CEMENTLESS HIP PROSTHESIS?

The FDA 510(k) record lists Mecron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Mecron Medical Products, 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 14 devices →

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.

↑