ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM
K-Number: K131093 · 2013-05-21
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Device Summary
Frequently Asked Questions
What is the ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM?
ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-05-21. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K131093.
When did ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM receive FDA 510(k) clearance?
ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM received FDA 510(k) clearance on 2013-05-21, under 510(k) number K131093.
Who is the listed applicant for ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM?
The FDA 510(k) record lists Wrightmedicaltechnologyinc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORTHOLOC(R) 3DI ANKLE PLATING SYSTEM?
The FDA product code for ORTHOLOC(R) 3DI ANKLE PLATING 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 Wrightmedicaltechnologyinc 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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