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FDA 510(k)

KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM

K-Number: K922824 · 1992-09-17

ApplicantJoint Medical Products Corp.
Decision Date1992-09-17
Product CodeHSX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM is the device name listed in this FDA 510(k) record. The listed applicant is Joint Medical Products Corp.. It received FDA 510(k) clearance on 1992-09-17 under 510(k) number K922824. 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 KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM?

KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM is a medical device that received FDA 510(k) clearance on 1992-09-17. The listed applicant is Joint Medical Products Corp.. The 510(k) number is K922824.

When did KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM receive FDA 510(k) clearance?

KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM received FDA 510(k) clearance on 1992-09-17, under 510(k) number K922824.

Who is the listed applicant for KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM?

The FDA 510(k) record lists Joint Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM?

The FDA product code for KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM is HSX.

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Other records listing Joint Medical Products Corp. as applicant

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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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