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FDA 510(k)

KT2000 KNEE LIGAMENT ARTHROMETER

K-Number: K942059 · 1994-09-20

ApplicantMedmetric Corp.
Decision Date1994-09-20
Product CodeLYH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KT2000 KNEE LIGAMENT ARTHROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medmetric Corp.. It received FDA 510(k) clearance on 1994-09-20 under 510(k) number K942059. The device is classified under product code LYH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KT2000 KNEE LIGAMENT ARTHROMETER?

KT2000 KNEE LIGAMENT ARTHROMETER is a medical device that received FDA 510(k) clearance on 1994-09-20. The listed applicant is Medmetric Corp.. The 510(k) number is K942059.

When did KT2000 KNEE LIGAMENT ARTHROMETER receive FDA 510(k) clearance?

KT2000 KNEE LIGAMENT ARTHROMETER received FDA 510(k) clearance on 1994-09-20, under 510(k) number K942059.

Who is the listed applicant for KT2000 KNEE LIGAMENT ARTHROMETER?

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

What is the FDA product code for KT2000 KNEE LIGAMENT ARTHROMETER?

The FDA product code for KT2000 KNEE LIGAMENT ARTHROMETER is LYH.

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.

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Other records listing Medmetric Corp. 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.

K943197KT1000/S KNEE LIGAMENT ARTHROMETERK904823FLEXERCYCLEK904898TORQUE FRAME QTF1000K854254TENSION-ISOMETERK812806KT-1000 DEVICEK812713DRAWER TEST

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Related Devices (Code: LYH)

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.

K943197KT1000/S KNEE LIGAMENT ARTHROMETERMedmetric Corp.K881876DYNAMIC CRUCIATE TESTERDyonics, Inc.K834462GENUCOMFar Orthopedics, Inc.K812806KT-1000 DEVICEMedmetric Corp.

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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