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FDA 510(k)

FUTURA TEXTURE-TRAKKED TOTAL HIP STEM

K-Number: K921382 · 1994-01-07

ApplicantArthronics, Inc.
Decision Date1994-01-07
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FUTURA TEXTURE-TRAKKED TOTAL HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Arthronics, Inc.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K921382. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUTURA TEXTURE-TRAKKED TOTAL HIP STEM?

FUTURA TEXTURE-TRAKKED TOTAL HIP STEM is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Arthronics, Inc.. The 510(k) number is K921382.

When did FUTURA TEXTURE-TRAKKED TOTAL HIP STEM receive FDA 510(k) clearance?

FUTURA TEXTURE-TRAKKED TOTAL HIP STEM received FDA 510(k) clearance on 1994-01-07, under 510(k) number K921382.

Who is the listed applicant for FUTURA TEXTURE-TRAKKED TOTAL HIP STEM?

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

What is the FDA product code for FUTURA TEXTURE-TRAKKED TOTAL HIP STEM?

The FDA product code for FUTURA TEXTURE-TRAKKED TOTAL HIP STEM is LWJ.

Related Clinical Trials

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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Other records listing Arthronics, 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.

K931107LOGYK ACETABULAR COMPONENT SYSTEM

Related Devices (Code: LWJ)

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.

K120595UNISYN PLUS HIP STEMConsensus Orthopedics, Inc.K103518TRINITY ACETABULAR SYSTEMCorin USAK090764NOVATION CFS PRESS-FIT AND CEMENTED STEMSExactech, Inc.K082146METHA SHORT STEM HIP SYSTEM XL FEMORAL HEADAesculap Implant Systems, Inc.K07006136MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTHayes Medical, Inc.K062978U2 HIP STEM, TI PLASMA SPRAYUnited Orthopedic Corp.

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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