EXACTECH EQUINOXE CAGE GLENOIDS
K-Number: K113309 · 2011-12-08
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Device Summary
Frequently Asked Questions
What is the EXACTECH EQUINOXE CAGE GLENOIDS?
EXACTECH EQUINOXE CAGE GLENOIDS is a medical device that received FDA 510(k) clearance on 2011-12-08. The listed applicant is Exactech, Inc.. The 510(k) number is K113309.
When did EXACTECH EQUINOXE CAGE GLENOIDS receive FDA 510(k) clearance?
EXACTECH EQUINOXE CAGE GLENOIDS received FDA 510(k) clearance on 2011-12-08, under 510(k) number K113309.
Who is the listed applicant for EXACTECH EQUINOXE CAGE GLENOIDS?
The FDA 510(k) record lists Exactech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXACTECH EQUINOXE CAGE GLENOIDS?
The FDA product code for EXACTECH EQUINOXE CAGE GLENOIDS is KWS.
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 Exactech, 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: KWS)
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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