RecallHawk

OsteoCoil™ Nitinol Compression System (Multiple Component PNs)

Flower Orthopedics Corporation Dba Conventus Flower Ortho

Summary

Flower Orthopedics Corporation Dba Conventus Flower Ortho received 510(k) clearance for OsteoCoil™ Nitinol Compression System (Multiple Component PNs), a HWC device. Cleared on 2024-11-22.

Details

Source

510(k) Clearance

External ID

K233567

Action Date

2024-11-22

Status

Traditional

Category

device

Product Code

HWC

Product Description

OsteoCoil™ Nitinol Compression System (Multiple Component PNs). Product code: HWC.

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 Flower Orthopedics Corporation Dba Conventus Flower Ortho have FDA actions?

This is the only FDA action we have on record for Flower Orthopedics Corporation Dba Conventus Flower Ortho in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K233567" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions