FDA 510(k) Applications Submitted by ORTHOCOR MEDICAL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121702 | 06/08/2012 | ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE | ORTHOCOR MEDICAL |
| K091996 | 07/02/2009 | ORTHOCOR KNEE SYSTEM BASIC | ORTHOCOR MEDICAL |
| K092044 | 07/06/2009 | ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE | ORTHOCOR MEDICAL |
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