FDA 510(k) Applications Submitted by Shanghai Iatrical-Ti Technologies Co Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K232996 | 09/22/2023 | Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) | Shanghai Iatrical-Ti Technologies Co Ltd. |
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