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 |