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FDA 510(k)

TECHMEDICA CONTINUUM HIP SYSTEM

K-Number: K931929 · 1994-03-29

ApplicantTechmedica, Inc.
Decision Date1994-03-29
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA CONTINUUM HIP 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 1994-03-29 under 510(k) number K931929. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDICA CONTINUUM HIP SYSTEM?

TECHMEDICA CONTINUUM HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Techmedica, Inc.. The 510(k) number is K931929.

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

TECHMEDICA CONTINUUM HIP SYSTEM received FDA 510(k) clearance on 1994-03-29, under 510(k) number K931929.

Who is the listed applicant for TECHMEDICA CONTINUUM HIP 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 TECHMEDICA CONTINUUM HIP SYSTEM?

The FDA product code for TECHMEDICA CONTINUUM HIP SYSTEM is LZO.

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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 COATINGK926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMK925420TECHMEDICA STANDARD BIPOLAR SYSTEMK923808MULLER STRAIGHT STEM FEMORAL PROSTHESISK926579TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE

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Related Devices (Code: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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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