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FDA 510(k)

CONTINUUM KNEE SYSTEM

K-Number: K920080 · 1992-09-01

ApplicantTechmedica, Inc.
Decision Date1992-09-01
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

CONTINUUM KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1992-09-01 under 510(k) number K920080. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CONTINUUM KNEE SYSTEM?

CONTINUUM KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Techmedica, Inc.. The 510(k) number is K920080.

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

CONTINUUM KNEE SYSTEM received FDA 510(k) clearance on 1992-09-01, under 510(k) number K920080.

Who is the listed applicant for CONTINUUM KNEE SYSTEM?

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

What is the FDA product code for CONTINUUM KNEE SYSTEM?

The FDA product code for CONTINUUM KNEE SYSTEM is JWH.

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Other records listing Techmedica, Inc. as applicant

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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.

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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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