QFP · Class II · 21 CFR 888.3090

FDA Product Code QFP: Intraoperative Orthopedic Strain Sensor

A Strain Sensor Device Is An Adjunct Tool Intended To Measure Strain On An Orthopedic Implant In The Intraoperative Setting Only. The Device Is Not Intended To Provide Diagnostic Information Or Influence Clinical Decision-making.

Leading manufacturers include Intellirod Spine, Inc..

Total

Cleared

379d

Avg days

2019

Since

FDA 510(k) Cleared Intraoperative Orthopedic Strain Sensor Devices (Product Code QFP)

1 devices

1–1 of 1

Not Cleared Mar 28, 2019

LOADPRO™ Intraoperative Rod Strain Sensor

DEN180012

Intellirod Spine, Inc.

Orthopedic · 379d

About Product Code QFP - Regulatory Context

Related FDA 510(k) Regulatory Insights

What is a Predicate Device in FDA 510(k)?
What is an FDA Product Code?
What is 510(k) Clearance?
Browse all Orthopedic FDA 510(k) clearances
FDA 510(k) regulatory consulting firms ranked by submission volume
FDA 510(k) submission cost and user fees FY 2026

Data Source

FDA 510(k) public files . 175,218 total devices indexed.

Latest clearance: Mar 28, 2019

Product Code Info

Code	QFP
Device class	Class II
CFR	21 CFR 888.3090
Panel	Orthopedic

Verify on FDA.gov

View QFP classification on FDA.gov →