The following data is part of a premarket notification filed by Acuity Surgical Devices, Llc with the FDA for A-link Z.
| Device ID | K201671 |
| 510k Number | K201671 |
| Device Name: | A-Link Z |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | Acuity Surgical Devices, LLC 8710 N Royal Lane Irving, TX 75063 |
| Contact | Bryan Cowan |
| Correspondent | Lucie Dalet Acknowledge Regulatory Strategies, LLC 2251 San Diego Ave, Suite B-257 San Diego, CA 92110 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-06-19 |
| Decision Date | 2021-05-04 |
| Summary: | summary |