MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR
K-Number: K844487 · 1985-02-19
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Device Summary
Frequently Asked Questions
What is the MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR?
MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR is a medical device that received FDA 510(k) clearance on 1985-02-19. The listed applicant is Mecron Medical Products, Inc.. The 510(k) number is K844487.
When did MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR receive FDA 510(k) clearance?
MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR received FDA 510(k) clearance on 1985-02-19, under 510(k) number K844487.
Who is the listed applicant for MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR?
The FDA 510(k) record lists Mecron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR?
The FDA product code for MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR is KWL.
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.
Related Devices (Code: KWL)
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.
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