ODI TALON INTRAMEDULLARY HIP NAIL
K-Number: K014189 · 2002-03-21
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Device Summary
Frequently Asked Questions
What is the ODI TALON INTRAMEDULLARY HIP NAIL?
ODI TALON INTRAMEDULLARY HIP NAIL is a medical device that received FDA 510(k) clearance on 2002-03-21. The listed applicant is Orthopedic Designs, Inc.. The 510(k) number is K014189.
When did ODI TALON INTRAMEDULLARY HIP NAIL receive FDA 510(k) clearance?
ODI TALON INTRAMEDULLARY HIP NAIL received FDA 510(k) clearance on 2002-03-21, under 510(k) number K014189.
Who is the listed applicant for ODI TALON INTRAMEDULLARY HIP NAIL?
The FDA 510(k) record lists Orthopedic Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ODI TALON INTRAMEDULLARY HIP NAIL?
The FDA product code for ODI TALON INTRAMEDULLARY HIP NAIL is JDS.
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 Orthopedic Designs, 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: JDS)
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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