JEIL BONE FIXATION SYSTEM
K-Number: K050669 · 2005-05-26
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Device Summary
Frequently Asked Questions
What is the JEIL BONE FIXATION SYSTEM?
JEIL BONE FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-26. The listed applicant is Jeil Medical Corporation. The 510(k) number is K050669.
When did JEIL BONE FIXATION SYSTEM receive FDA 510(k) clearance?
JEIL BONE FIXATION SYSTEM received FDA 510(k) clearance on 2005-05-26, under 510(k) number K050669.
Who is the listed applicant for JEIL BONE FIXATION SYSTEM?
The FDA 510(k) record lists Jeil Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JEIL BONE FIXATION SYSTEM?
The FDA product code for JEIL BONE FIXATION SYSTEM is JEY.
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 Jeil Medical Corporation 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: JEY)
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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