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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K101823
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Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching 2 05/05/2017 Arthrex, Inc.
Anthrex PEEK SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm 2 05/05/2017 Arthrex, Inc.
Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching 2 05/05/2017 Arthrex, Inc.
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