510(k) K222015

Device
Integral Titanium Cervical Interbody
Applicant
Nvision Biomedical Technologies, Inc.
510(k) number
K222015
Product code
ODP
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-05
Date received
2022-07-08
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Diana Langham
Address
4590 Lockhill Selma San Antonio TX US 78249 78249

FDA Registration Numbers

Source Documents

510(k) summary PDF

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