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FDA 510(k)

CKS POROUS COATED FEMORAL COMPONENT

K-Number: K933935 · 1994-10-11

ApplicantTechmedica, Inc.
Decision Date1994-10-11
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CKS POROUS COATED FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1994-10-11 under 510(k) number K933935. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CKS POROUS COATED FEMORAL COMPONENT?

CKS POROUS COATED FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 1994-10-11. The listed applicant is Techmedica, Inc.. The 510(k) number is K933935.

When did CKS POROUS COATED FEMORAL COMPONENT receive FDA 510(k) clearance?

CKS POROUS COATED FEMORAL COMPONENT received FDA 510(k) clearance on 1994-10-11, under 510(k) number K933935.

Who is the listed applicant for CKS POROUS COATED FEMORAL COMPONENT?

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 CKS POROUS COATED FEMORAL COMPONENT?

The FDA product code for CKS POROUS COATED FEMORAL COMPONENT is HRY.

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Other records listing Techmedica, Inc. as applicant

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Related Devices (Code: HRY)

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.

K193549SIGMA High Performance (HP) Partial Knee SystemDepuy Ireland UCK190633NanoOrtho NanoKnee® SystemNanoortho, LLCK152631MPO Total Knee Systems MR LabelingMicroport Orthopedics, Inc.K131167UNIVATIONAesculap Implant Systems, LLCK122277OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (OXFORD TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEMBiomet Manufacturing CorpK110415SIGNATURE PLANNER / SIGNATURE GUIDESMaterialise NV

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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