510(k) K061067 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
TRABECULAR METAL ACETABULAR AUGMENTS
| Applicant | Zimmer Trabecular, Allendale NJ, US |
| Decision | Substantially Equivalent, May 25, 2006 |
| Received | Apr 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061067
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 12, 2010 | Zimmer Inc. Trabecular Metal acetabular revision system buttress augment size, 54, 00-4898-001-54, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address bony deficiencies of Terminated |
LPH | None listed |
| Aug 12, 2010 | Zimmer Inc. Trabecular Metal acetabular revision system buttress augment size, 58, 00-4898-001-58, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address bony deficiencies of Terminated |
LPH | None listed |
| Aug 12, 2010 | Zimmer Inc. Trabecular Metal acetabular revision system column buttress left posterior/right anterior, 00-4894-300-00, sterile, Zimmer Inc., Parsippany, NJ.
Usage: Implantable devices that are used to address b Terminated |
LPH | None listed |
| Aug 12, 2010 | Zimmer Inc. Trabecular Metal acetabular revision system column buttress right posterior/left anterior, 00-4894-400-00, sterile, Zimmer Inc., Parsippany, NJ. Terminated |
LPH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.