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FDA 510(k)

CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT

K-Number: K031859 · 2004-02-18

ApplicantArthrosurface, Inc.
Decision Date2004-02-18
Product CodeKWD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Arthrosurface, Inc.. It received FDA 510(k) clearance on 2004-02-18 under 510(k) number K031859. The device is classified under product code KWD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT?

CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT is a medical device that received FDA 510(k) clearance on 2004-02-18. The listed applicant is Arthrosurface, Inc.. The 510(k) number is K031859.

When did CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT receive FDA 510(k) clearance?

CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT received FDA 510(k) clearance on 2004-02-18, under 510(k) number K031859.

Who is the listed applicant for CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT?

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

What is the FDA product code for CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT?

The FDA product code for CAP GREAT TOE RESURFACING HEMI-ARTHROPLASTY IMPLANT is KWD.

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Other records listing Arthrosurface, 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.

K203375OVOMotion Reverse Shoulder Arthroplasty SystemK200718Arthrosurface WristMotion Total Wrist Arthroplasty SystemK190261BOSS Toe Fixation SystemK181280Patello-Femoral Wave (Kahuna) Arthroplasty SystemK173964OVOMotion Shoulder Arthroplasty SystemK172383Arthrosurface Bone Screws

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Related Devices (Code: KWD)

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.

K250074HYALEX® MTP Hemiarthroplasty ImplantHyalex Orthopaedics, Inc.K240268Accu-Joint Hemi ImplantAccufix Surgical, Inc.K221220Montross Extremity Medical Hemi Implant SystemMontross Extremity MedicalK222964BioPoly Lesser Toe Hemiarthroplasty ImplantBioPoly, LLCK201393restor3d MTP ImplantRestor3D, Inc.K203634BioPoly Great Toe Hemiarthroplasty ImplantBioPoly, LLC

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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