CEMENT OBTURATOR
FDA product code LZN · Class 2 · 16 devices · 37 reports · 7 devices named in recalls
- BIOSTOP 5463-12-000Depuy Orthopaedics, Inc. · CEMENT OBTURATOR1 recall6 reports
- BIOSTOP 5463-08-000Depuy Orthopaedics, Inc. · CEMENT OBTURATOR1 recall1 report
- BIOSTOP 5463-16-000Depuy Orthopaedics, Inc. · CEMENT OBTURATOR1 recall1 report
- BIOSTOP 5463-18-000Depuy Orthopaedics, Inc. · CEMENT OBTURATOR1 recall1 report
- ACM BioPrep 0306705000Stryker Corporation · CEMENT OBTURATOR1 recall0 reports
- NA 0306703000Stryker Corporation · CEMENT OBTURATOR1 recall0 reports
- BIOSTOP 5463-20-000Depuy Orthopaedics, Inc. · CEMENT OBTURATOR1 recall0 reports
- PREP-IM 121010Smith & Nephew, Inc. · CEMENT OBTURATOR10 reports
- CEMENT RESTRICTOR EBO102Tornier · CEMENT OBTURATOR8 reports
- BUCK 129419Smith & Nephew, Inc. · CEMENT OBTURATOR2 reports
- EXETER 0939-0-116Howmedica Osteonics Corp. · CEMENT OBTURATOR2 reports
- Bone Plug 6215-5-011Howmedica Osteonics Corp. · CEMENT OBTURATOR2 reports
- DJO SURGICAL 415-00-120Encore Medical, L.P. · CEMENT OBTURATOR1 report
- DJO SURGICAL 415-00-140Encore Medical, L.P. · CEMENT OBTURATOR1 report
- NA 8011-20-20Zimmer, Inc. · CEMENT OBTURATOR1 report
- BUCK 129418Smith & Nephew, Inc. · CEMENT OBTURATOR1 report