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Neuro Plating System, Neuro Plating System Plates(NST304M02A and 61 Models), Neuro Plating System-Packaging unit(NSP-001

Osteonic Co., Ltd.

Summary

Osteonic Co., Ltd. received 510(k) clearance for Neuro Plating System, Neuro Plating System Plates(NST304M02A and 61 Models), Neuro Plating System-Packaging unit(NSP-001 and 10 models), Neuro Plating System-Sterile Kit(TCN-011 and 69 models), Neuro Plating System-Screws(N15A03 and 11 models), a GWO device. Cleared on 2022-01-27.

Details

Source

510(k) Clearance

External ID

K210360

Action Date

2022-01-27

Status

Traditional

Category

device

Product Code

GWO

Product Description

Neuro Plating System, Neuro Plating System Plates(NST304M02A and 61 Models), Neuro Plating System-Packaging unit(NSP-001 and 10 models), Neuro Plating System-Sterile Kit(TCN-011 and 69 models), Neuro Plating System-Screws(N15A03 and 11 models). Product code: GWO.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Osteonic Co., Ltd. has received 10 total clearances in our database.

Osteonic Co., Ltd. has 10 FDA actions in our database, including 10 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Osteonic Co., Ltd. have FDA actions?

Osteonic Co., Ltd. has 10 FDA actions in our database, including 0 recalls and 10 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K210360" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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