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FDA 510(k) Applications for Medical Device Product Code "MTZ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K973552 | BIO-VASCULAR, INC. | OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP | 12/16/1997 |
K023643 | MACROPORE BIOSURGERY, INC. | MACROPORE SURGICAL BARRIER FILM | 02/21/2003 |