FDA Device Intelligence
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Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive

FDA product code PBI · Class 2 · Orthopedic

1,528
Registered devices
2,276
Adverse events
2
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-05-07Biomet, Inc.Guide rod may fracture during impaction of the acetabular shell and be retained in the inserter or the patient and could result in a delay in surgery.
2014-05-07Biomet, Inc.Guide rod may fracture during impaction of the acetabular shell and be retained in the inserter or the patient and could result in a delay in surgery.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.