FDA 510(k) Applications Submitted by IMPLANTS INTERNATIONAL, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071583 | 06/08/2007 | CERMET III ACETABULAR CUP SYSTEM | IMPLANTS INTERNATIONAL, LTD |
| K132539 | 08/13/2013 | RING-LOK MODULAR BIPOLAR SYSTEM | IMPLANTS INTERNATIONAL, LTD |
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