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FDA 510(k)

ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY

K-Number: K063251 · 2007-01-24

ApplicantZimmer, Inc.
Decision Date2007-01-24
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2007-01-24 under 510(k) number K063251. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY?

ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY is a medical device that received FDA 510(k) clearance on 2007-01-24. The listed applicant is Zimmer, Inc.. The 510(k) number is K063251.

When did ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY receive FDA 510(k) clearance?

ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY received FDA 510(k) clearance on 2007-01-24, under 510(k) number K063251.

Who is the listed applicant for ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY?

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 ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY?

The FDA product code for ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY is KWA.

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Other records listing Zimmer, Inc. as applicant

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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: KWA)

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.

K122778PROFEMUR Z REVISION HIP STEMWrightmedicaltechnologyincK121544DYNASTY BIOFOAM SHELLWrightmedicaltechnologyincK113271METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONSBiomet Manufacturing, Inc.K113322CONSERVE THIN SHELLWrightmedicaltechnologyincK112080PRESERVE HIP STEMWrightmedicaltechnologyincK112150PROFEMUR GLADIATOR HA HIP STEMWrightmedicaltechnologyinc

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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