ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM
K-Number: K033878 · 2004-02-20
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Device Summary
Frequently Asked Questions
What is the ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM?
ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2004-02-20. The listed applicant is Depuy Ace. The 510(k) number is K033878.
When did ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM receive FDA 510(k) clearance?
ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM received FDA 510(k) clearance on 2004-02-20, under 510(k) number K033878.
Who is the listed applicant for ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM?
The FDA 510(k) record lists Depuy Ace as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACE ANTEGRADE RETROGRADE HUMERAL NAIL SYSTEM?
The FDA product code for ACE ANTEGRADE RETROGRADE HUMERAL 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 Depuy Ace 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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