510(k) K800894 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
DUPUY CEMENT RESTRICTOR TRIALS & INSTR.
| Applicant | Depuy, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 2, 1980 |
| Received | Apr 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800894
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 17, 2011 | Depuy Orthopaedics, Inc. DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 1, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio Terminated |
JDK | None listed |
| Mar 17, 2011 | Depuy Orthopaedics, Inc. DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 4, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio Terminated |
JDK | None listed |
| Mar 17, 2011 | Depuy Orthopaedics, Inc. DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantatio Terminated |
JDK | None listed |
| Mar 17, 2011 | Depuy Orthopaedics, Inc. DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 3, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantati Terminated |
JDK | None listed |
| Mar 17, 2011 | Depuy Orthopaedics, Inc. DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This device is intended to restrict bone cement migration into the distal medullary canal during implantati Terminated |
JDK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.