MULTIDIRECTIONAL THREADED PEG
K-Number: K060864 · 2006-04-28
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Device Summary
Frequently Asked Questions
What is the MULTIDIRECTIONAL THREADED PEG?
MULTIDIRECTIONAL THREADED PEG is a medical device that received FDA 510(k) clearance on 2006-04-28. The listed applicant is Hand Innovations, LLC. The 510(k) number is K060864.
When did MULTIDIRECTIONAL THREADED PEG receive FDA 510(k) clearance?
MULTIDIRECTIONAL THREADED PEG received FDA 510(k) clearance on 2006-04-28, under 510(k) number K060864.
Who is the listed applicant for MULTIDIRECTIONAL THREADED PEG?
The FDA 510(k) record lists Hand Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIDIRECTIONAL THREADED PEG?
The FDA product code for MULTIDIRECTIONAL THREADED PEG is LXT.
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 Hand Innovations, LLC 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: LXT)
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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