FDA 510(k) Applications Submitted by DAVID ROTHKOPF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101279 | 05/06/2010 | CORRIDOR4DM V2010 MODEL: V2010 | INVIA |
| K121702 | 06/08/2012 | ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE | ORTHOCOR MEDICAL |
| K113084 | 10/18/2011 | RENOVIS CANNULATED SCREW SYSTEM | RENOVIS SURGICAL TECHNOLOGIES, LLC |
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