APEX INTRAMEDULLARY NAIL SYSTEM
K-Number: K020562 · 2002-05-16
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Device Summary
Frequently Asked Questions
What is the APEX INTRAMEDULLARY NAIL SYSTEM?
APEX INTRAMEDULLARY NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-05-16. The listed applicant is Magly Orthopedics, LLC. The 510(k) number is K020562.
When did APEX INTRAMEDULLARY NAIL SYSTEM receive FDA 510(k) clearance?
APEX INTRAMEDULLARY NAIL SYSTEM received FDA 510(k) clearance on 2002-05-16, under 510(k) number K020562.
Who is the listed applicant for APEX INTRAMEDULLARY NAIL SYSTEM?
The FDA 510(k) record lists Magly Orthopedics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APEX INTRAMEDULLARY NAIL SYSTEM?
The FDA product code for APEX INTRAMEDULLARY NAIL SYSTEM is HSB.
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 Magly Orthopedics, LLC 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: HSB)
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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