ABG II MODULAR HIP STEM
K-Number: K092406 · 2009-11-04
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Device Summary
Frequently Asked Questions
What is the ABG II MODULAR HIP STEM?
ABG II MODULAR HIP STEM is a medical device that received FDA 510(k) clearance on 2009-11-04. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K092406.
When did ABG II MODULAR HIP STEM receive FDA 510(k) clearance?
ABG II MODULAR HIP STEM received FDA 510(k) clearance on 2009-11-04, under 510(k) number K092406.
Who is the listed applicant for ABG II MODULAR HIP STEM?
The FDA 510(k) record lists Howmedica Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABG II MODULAR HIP STEM?
The FDA product code for ABG II MODULAR HIP STEM is MEH.
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 Howmedica Osteonics Corp. 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: MEH)
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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