FDA 510(k) Applications Submitted by Orthosoft, Inc (d/b/a Zimmer CAS)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230180 | 01/23/2023 | Rosa Knee System | Orthosoft, Inc (d/b/a Zimmer CAS) |
| K213708 | 11/24/2021 | ROSA« Knee System | Orthosoft, Inc (d/b/a Zimmer CAS) |
| K231162 | 04/24/2023 | ROSA Hip System | Orthosoft, Inc (d/b/a Zimmer CAS) |
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