FDA 510(k) Applications Submitted by SPINE NEXT AMERICA CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K042714 | 09/24/2004 | FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 1, 2, 3 AND 4 | SPINE NEXT AMERICA CORPORATION |
| K042713 | 09/30/2004 | FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5 | SPINE NEXT AMERICA CORPORATION |
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