Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0412-2013 — Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Inspan implants into the spinous process bone, resulting in fixation of the implant.

U.S. FDA — Device Enforcement · United States · 2012-08-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0412-2013
Date of alert
2012-08-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
SpineFrontier, Inc.
Product category
device
Product type
Devices
Reported risk: Inspan Compressors may break at weld causing a loss of compression
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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