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FDA 510(k)

SnapHammer Hammertoe Correction System

K-Number: K231453 · 2024-02-16

ApplicantNvision Biomedical Technologies, Inc.
Decision Date2024-02-16
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SnapHammer Hammertoe Correction System is a medical device manufactured by Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2024-02-16 under approval number K231453. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SnapHammer Hammertoe Correction System?

SnapHammer Hammertoe Correction System is a medical device that received FDA 510(k) clearance on 2024-02-16. It is manufactured by Nvision Biomedical Technologies, Inc.. The 510(k) number is K231453.

When was SnapHammer Hammertoe Correction System approved by the FDA?

SnapHammer Hammertoe Correction System received FDA 510(k) clearance on 2024-02-16, under approval number K231453.

What company makes SnapHammer Hammertoe Correction System?

SnapHammer Hammertoe Correction System is manufactured by Nvision Biomedical Technologies, Inc..

What is the FDA product code for SnapHammer Hammertoe Correction System?

The FDA product code for SnapHammer Hammertoe Correction System is HWC. This falls under the Cardiovascular category.

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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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