FDA 510(k) Applications Submitted by K7 LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133103 | 09/30/2013 | AVERSION PEDICLE SCREW SYSTEM | K7 LLC |
| K133126 | 09/30/2013 | K7 LUMBAR SPACERS | K7 LLC |
| K123388 | 11/02/2012 | K7C SPACER | K7 LLC |
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