Devices

Device Recall Single Use PERPOS PLS System

Model / Serial
Lot#090907A
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide distribution: USA (nationwide) including states of: CA, FL, MO, NY, OH, PA, TN, WA, and WI; and country of: Europe.
Product Description
Single Use PERPOS PLS System, Catalog #9045-01 || Catalog#9045-01 for Single Use PERPOS PLS System- a sterile, medical device kit consisting of the components: PERPOS Access Needle, PERPOS K-Wires, PERPOS 2-in-1 Drill, PERPOS Tap, PERPOS Device Driver, 4.5mm BONE-LOK PLS Implant, and PERPOS Pull Pin Remover. The kit is used by medical professions to stablize the spine as an aid to fusion through immobilization of the facet joints.
Manufacturer
Interventional Spine Inc
1 Event
- Recall of Device Recall Single Use PERPOS PLS System

Manufacturer

Interventional Spine Inc

Manufacturer Address
Interventional Spine Inc, 13700 Alton Pkwy Ste 160, Irvine CA 92618-1618
Manufacturer Parent Company (2017)
Interventional Spine Inc.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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