RecallHawk

Camber Spine Navigation System

Camber Spine Technologies

Summary

Camber Spine Technologies received 510(k) clearance for Camber Spine Navigation System, a OLO device. Cleared on 2022-04-29.

Details

Source

510(k) Clearance

External ID

K220038

Action Date

2022-04-29

Status

Traditional

Category

device

Product Code

OLO

Product Description

Camber Spine Navigation System. Product code: OLO.

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. Camber Spine Technologies has received 5 total clearances in our database.

Camber Spine Technologies has 5 FDA actions in our database, including 5 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 Camber Spine Technologies have FDA actions?

Camber Spine Technologies has 5 FDA actions in our database, including 0 recalls and 5 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K220038" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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