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U.S. Department of Health and Human Services

Class 2 Device Recall SPINE BUTTRESS (FANG) PLATE SYSTEM

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  Class 2 Device Recall SPINE BUTTRESS (FANG) PLATE SYSTEM see related information
Date Initiated by Firm February 20, 2013
Date Posted May 27, 2013
Recall Status1 Terminated 3 on March 26, 2014
Recall Number Z-1418-2013
Recall Event ID 64586
510(K)Number K090415  
Product Classification Appliance, fixation, spinal intervertebral body - Product Code KWQ
Product Fang Screw 20mm
Fang Plate 21mm

Product Usage:
Spinal Solutions distributes a variety of spinal fixation devices in loaner bins or on consignment. The company has decided to provide directions for use and surgical techniques electronically on the companys website. The company has created a label intended to inform the user of the existence of the websites and the information it contains. Indications for use: multiple.
Code Information Item # FP1220 FP1221 
Recalling Firm/
Manufacturer		 Spinal Solutions, LLC
26157 Jefferson Ave
Murrieta CA 92562-9561
For Additional Information Contact
951-304-9001
Manufacturer Reason
for Recall		 The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Spinal Solutions because the directions for use and surgical techniques were not being provided to every physician and for every surgery.
FDA Determined
Cause 2		 Labeling design
Action Spinal Solutions sent a recall letter dated March 8, 2013 to all customers who purchased loaner bins and sterilization trays for implants and instruments from Spinal Solutions. The letter identified the affected product, problem identified and actions to be taken. Customers are instructed to call the office at the number (951) 304-9001 if they are requesting paper copies of any of the literature.
Quantity in Commerce 16 units
Distribution USA Nationwide Distribution in the states of MS: TX, NV, CA, MD, and WI.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = KWQ and Original Applicant = EMINENT SPINE
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