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FDA 510(k)

NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM

K-Number: K022324 · 2002-09-17

Decision Date2002-09-17
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Osteomedics, Inc.. It received FDA 510(k) clearance on 2002-09-17 under 510(k) number K022324. 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 NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM?

NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-17. The listed applicant is Osteomedics, Inc.. The 510(k) number is K022324.

When did NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM receive FDA 510(k) clearance?

NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM received FDA 510(k) clearance on 2002-09-17, under 510(k) number K022324.

Who is the listed applicant for NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM?

The FDA 510(k) record lists Osteomedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM?

The FDA product code for NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW 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 Osteomedics, 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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