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FDA 510(k)

LFIC OR FETTO HIP

K-Number: K952776 · 1996-02-14

ApplicantZimmer, Inc.
Decision Date1996-02-14
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LFIC OR FETTO HIP is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1996-02-14 under 510(k) number K952776. 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 LFIC OR FETTO HIP?

LFIC OR FETTO HIP is a medical device that received FDA 510(k) clearance on 1996-02-14. The listed applicant is Zimmer, Inc.. The 510(k) number is K952776.

When did LFIC OR FETTO HIP receive FDA 510(k) clearance?

LFIC OR FETTO HIP received FDA 510(k) clearance on 1996-02-14, under 510(k) number K952776.

Who is the listed applicant for LFIC OR FETTO HIP?

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

What is the FDA product code for LFIC OR FETTO HIP?

The FDA product code for LFIC OR FETTO HIP is LWJ.

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Other records listing Zimmer, 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.

K262955OsseoFit Stemless Shoulder SystemK260831Z1 Hip SystemK261683Augment Off-Axis Instrument SystemK251840Zimmer® Persona® Personalized Knee SystemK260182Avenir® Müller Stem; Avenir Complete™ Hip SystemK253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)

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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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