FDA 510(k) Applications Submitted by Cartiva, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142490 | 09/04/2014 | ProxiFuse Hammer Toe Device | Cartiva, Inc. |
| K192156 | 08/09/2019 | Cartiva SCI instrumentation set | Cartiva, Inc. |
| K181348 | 05/21/2018 | Cartiva SCI Disposable Instrumentation Set | Cartiva, Inc. |
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