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FDA 510(k)

F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM

K-Number: K935990 · 1994-07-13

ApplicantImplex Corp.
Decision Date1994-07-13
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Implex Corp.. It received FDA 510(k) clearance on 1994-07-13 under 510(k) number K935990. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM?

F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM is a medical device that received FDA 510(k) clearance on 1994-07-13. The listed applicant is Implex Corp.. The 510(k) number is K935990.

When did F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM receive FDA 510(k) clearance?

F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM received FDA 510(k) clearance on 1994-07-13, under 510(k) number K935990.

Who is the listed applicant for F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM?

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

What is the FDA product code for F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM?

The FDA product code for F-220 PRESS-FIT FEMORAL HIP STEM SYSTEM is MEH.

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Other records listing Implex Corp. as applicant

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Related Devices (Code: MEH)

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.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, Inc.

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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