OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM
K-Number: K062863 · 2006-10-31
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Device Summary
Frequently Asked Questions
What is the OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM?
OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-31. The listed applicant is Osteomed LP. The 510(k) number is K062863.
When did OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM receive FDA 510(k) clearance?
OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM received FDA 510(k) clearance on 2006-10-31, under 510(k) number K062863.
Who is the listed applicant for OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM?
The FDA 510(k) record lists Osteomed LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM?
The FDA product code for OSTEOMED EXTENDED 2.0/2.4CANNULATED SCREW SYSTEM is HWC. This falls under the Cardiovascular category.
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 Osteomed LP 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: HWC)
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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