RecallHawk

StageOne™ Select Hip Cement Spacer Molds

Biomet, Inc.

Summary

Biomet, Inc. received 510(k) clearance for StageOne™ Select Hip Cement Spacer Molds, a MBB device. Cleared on 2022-12-28.

Details

Source

510(k) Clearance

External ID

K222760

Action Date

2022-12-28

Status

Traditional

Category

device

Product Code

MBB

Product Description

StageOne™ Select Hip Cement Spacer Molds. Product code: MBB.

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. Biomet, Inc. has received 6 total clearances in our database.

Biomet, Inc. has 66 FDA actions in our database, including 60 recalls and 6 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 Biomet, Inc. have FDA actions?

Biomet, Inc. has 66 FDA actions in our database, including 60 recalls and 6 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K222760" 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