ASCENSION ANKLE FUSION PLATE SYSTEM
K-Number: K100176 · 2010-06-16
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Device Summary
Frequently Asked Questions
What is the ASCENSION ANKLE FUSION PLATE SYSTEM?
ASCENSION ANKLE FUSION PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-06-16. The listed applicant is Ascension Orthopedics, Inc.. The 510(k) number is K100176.
When did ASCENSION ANKLE FUSION PLATE SYSTEM receive FDA 510(k) clearance?
ASCENSION ANKLE FUSION PLATE SYSTEM received FDA 510(k) clearance on 2010-06-16, under 510(k) number K100176.
Who is the listed applicant for ASCENSION ANKLE FUSION PLATE SYSTEM?
The FDA 510(k) record lists Ascension Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASCENSION ANKLE FUSION PLATE SYSTEM?
The FDA product code for ASCENSION ANKLE FUSION PLATE SYSTEM is HRS.
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 Ascension Orthopedics, 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: HRS)
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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