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FDA 510(k)

MODULAR FOOT SYSTEM

K-Number: K073624 · 2008-03-20

Decision Date2008-03-20
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODULAR FOOT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Orthohelix Surgical Designs, Inc.. It received FDA 510(k) clearance on 2008-03-20 under 510(k) number K073624. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR FOOT SYSTEM?

MODULAR FOOT SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-20. The listed applicant is Orthohelix Surgical Designs, Inc.. The 510(k) number is K073624.

When did MODULAR FOOT SYSTEM receive FDA 510(k) clearance?

MODULAR FOOT SYSTEM received FDA 510(k) clearance on 2008-03-20, under 510(k) number K073624.

Who is the listed applicant for MODULAR FOOT SYSTEM?

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 MODULAR FOOT SYSTEM?

The FDA product code for MODULAR FOOT 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 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.

View all 21 devices →

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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