FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

A-Link Z

K Number: K201671 · Decision May 4, 2021
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
8
Review Days
319

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Basic Information

Device Name
A-Link Z
K Number
K201671
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acuity Surgical Devices, LLC
Date Received
June 19, 2020
Decision Date
May 4, 2021
Product Code
OVD
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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Other Clearances by Acuity Surgical Devices, LLC

K Number Device Name
K251735 Stabilis SA Cervical Stand-Alone System (Various PNs)
K251335 Tera Lumbar Interbody Fusion System (Various PNs)
K243386 Ventris Intervertebral Body Fusion Device
K241413 sagAlign Lumbar Cage System (Various PNs)
K230639 Align Cervical Interbody Fusion System
K222561 Align
K221535 Align Lumbar Interbody Fusion System