FDA 510(k) Applications Submitted by OrthoCircle Spine d.b.a. OC Medical Devices
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222799 | 09/16/2022 | Haymaker« Screw System | OrthoCircle Spine d.b.a. OC Medical Devices |
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