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FDA 510(k)

STELKAST UNICONDYLAR KNEE SYSTEM

K-Number: K032824 · 2003-11-13

Decision Date2003-11-13
Product CodeHSX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STELKAST UNICONDYLAR KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stelkast Company. It received FDA 510(k) clearance on 2003-11-13 under 510(k) number K032824. The device is classified under product code HSX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STELKAST UNICONDYLAR KNEE SYSTEM?

STELKAST UNICONDYLAR KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2003-11-13. The listed applicant is Stelkast Company. The 510(k) number is K032824.

When did STELKAST UNICONDYLAR KNEE SYSTEM receive FDA 510(k) clearance?

STELKAST UNICONDYLAR KNEE SYSTEM received FDA 510(k) clearance on 2003-11-13, under 510(k) number K032824.

Who is the listed applicant for STELKAST UNICONDYLAR KNEE SYSTEM?

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

What is the FDA product code for STELKAST UNICONDYLAR KNEE SYSTEM?

The FDA product code for STELKAST UNICONDYLAR KNEE SYSTEM is HSX.

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 Stelkast Company 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 40 devices →

Related Devices (Code: HSX)

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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