FDA 510(k) Applications Submitted by YAYORI FUJIMAKI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132241 | 07/18/2013 | GRYPHON BR ANCHOR W/ PROKNOT TECHNOLOGY, GRYPHON BR ANCHOR W/ PROKNOT TECHNOLOGY - HIP, GRYPHON PEEK ANCHOR W/ PROKNOT T | DEPUY MITEK, A JOHNSON & JOHNSON COMPANY |
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