EDGELOCK
K-Number: K093900 · 2010-02-17
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Device Summary
Frequently Asked Questions
What is the EDGELOCK?
EDGELOCK is a medical device that received FDA 510(k) clearance on 2010-02-17. The listed applicant is Orthohelix Surgical Designs, Inc.. The 510(k) number is K093900.
When did EDGELOCK receive FDA 510(k) clearance?
EDGELOCK received FDA 510(k) clearance on 2010-02-17, under 510(k) number K093900.
Who is the listed applicant for EDGELOCK?
The FDA 510(k) record lists Orthohelix Surgical Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EDGELOCK?
The FDA product code for EDGELOCK 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 Orthohelix Surgical 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: 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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