RecallHawk

Sterile Posterior Spinal Fixation System

Shanghai Reach Medical Instrument Co, Ltd.

Summary

Shanghai Reach Medical Instrument Co, Ltd. received 510(k) clearance for Sterile Posterior Spinal Fixation System, a NKB device. Cleared on 2022-08-31.

Details

Source

510(k) Clearance

External ID

K221745

Action Date

2022-08-31

Status

Special

Category

device

Product Code

NKB

Product Description

Sterile Posterior Spinal Fixation System. Product code: NKB.

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. Shanghai Reach Medical Instrument Co, Ltd. has received 2 total clearances in our database.

Shanghai Reach Medical Instrument Co, Ltd. has 2 FDA actions in our database, including 2 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 Shanghai Reach Medical Instrument Co, Ltd. have FDA actions?

Shanghai Reach Medical Instrument Co, Ltd. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K221745" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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