FDA 510(k) Applications for Medical Device Product Code "NXM"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K090078 | IOP, INC. | KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT | 05/08/2009 |
K053622 | IOP, INC. | SURGISIS OCULAR GRAFT | 03/15/2006 |