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FDA 510(k)

PROVEN MODULAR TIBIAL TRAY

K-Number: K030577 · 2003-03-25

Decision Date2003-03-25
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROVEN MODULAR TIBIAL TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Stelkast Company. It received FDA 510(k) clearance on 2003-03-25 under 510(k) number K030577. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROVEN MODULAR TIBIAL TRAY?

PROVEN MODULAR TIBIAL TRAY is a medical device that received FDA 510(k) clearance on 2003-03-25. The listed applicant is Stelkast Company. The 510(k) number is K030577.

When did PROVEN MODULAR TIBIAL TRAY receive FDA 510(k) clearance?

PROVEN MODULAR TIBIAL TRAY received FDA 510(k) clearance on 2003-03-25, under 510(k) number K030577.

Who is the listed applicant for PROVEN MODULAR TIBIAL TRAY?

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 PROVEN MODULAR TIBIAL TRAY?

The FDA product code for PROVEN MODULAR TIBIAL TRAY is JWH.

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: JWH)

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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