RecallHawk

Fortilink with TiPlus Technology

Paradigm Spine

Summary

Paradigm Spine received 510(k) clearance for Fortilink with TiPlus Technology, a ODP device. Cleared on 2022-01-27.

Details

Source

510(k) Clearance

External ID

K213493

Action Date

2022-01-27

Status

Traditional

Category

device

Product Code

ODP

Product Description

Fortilink with TiPlus Technology. Product code: ODP.

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.

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 Paradigm Spine have FDA actions?

This is the only FDA action we have on record for Paradigm Spine in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K213493" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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