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FDA 510(k)

ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))

K-Number: K896542 · 1990-02-15

ApplicantTechmedica, Inc.
Decision Date1990-02-15
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1990-02-15 under 510(k) number K896542. 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 ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))?

ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Techmedica, Inc.. The 510(k) number is K896542.

When did ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) receive FDA 510(k) clearance?

ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) received FDA 510(k) clearance on 1990-02-15, under 510(k) number K896542.

Who is the listed applicant for ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))?

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 ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))?

The FDA product code for ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) is JWH.

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Other records listing Techmedica, Inc. 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.

K933935CKS POROUS COATED FEMORAL COMPONENTK932017TECHMEDICA CONTINUUM HIP WITH HA COATINGK931929TECHMEDICA CONTINUUM HIP SYSTEMK926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMK925420TECHMEDICA STANDARD BIPOLAR SYSTEMK923808MULLER STRAIGHT STEM FEMORAL PROSTHESIS

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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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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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