RecallHawk

Summary

Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics received 510(k) clearance for TaperSet™ Hip System, a LPH device. Cleared on 2025-11-20.

Details

Source

510(k) Clearance

External ID

K252846

Action Date

2025-11-20

Status

Special

Category

device

Product Code

LPH

Product Description

TaperSet™ Hip System. Product code: LPH.

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. Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics has received 2 total clearances in our database.

Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics 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 Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics have FDA actions?

Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics 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 "K252846" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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