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FDA 510(k)

MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN.

K-Number: K910664 · 1992-04-01

ApplicantMedimix Products, Inc.
Decision Date1992-04-01
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. is the device name listed in this FDA 510(k) record. The listed applicant is Medimix Products, Inc.. It received FDA 510(k) clearance on 1992-04-01 under 510(k) number K910664. 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 MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN.?

MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. is a medical device that received FDA 510(k) clearance on 1992-04-01. The listed applicant is Medimix Products, Inc.. The 510(k) number is K910664.

When did MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. receive FDA 510(k) clearance?

MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. received FDA 510(k) clearance on 1992-04-01, under 510(k) number K910664.

Who is the listed applicant for MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN.?

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

What is the FDA product code for MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN.?

The FDA product code for MOD. TROCHANTER SCREW & WASHER W/ ANODIZED TITAN. is LWJ.

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Other records listing Medimix Products, 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.

K914733TTL MEDICATED DRESSINGK902772PLEASURE PLUSK860113DOUBLE-JECT TRANSFER NEEDLE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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