FDA 510(k) Applications for Medical Device Product Code "OXK"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K121289 | LIFECELL CORP. | LTM-LABAROSCOPIC SURGICAL MESH | 08/03/2012 |
| K130817 | LIFECELL CORP. | LTN - LAPAROSCOPIC SURGICAL MESH | 04/17/2013 |
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