Last synced on 30 May 2025 at 11:05 pm

SeaSpine Vu a•POD Prime NanoMetalene Intervertebral Body Fusion Device, SeaSpine Vu a•POD Prime Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173606
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2018
Days to Decision
143 days
Submission Type
Summary

SeaSpine Vu a•POD Prime NanoMetalene Intervertebral Body Fusion Device, SeaSpine Vu a•POD Prime Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173606
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2018
Days to Decision
143 days
Submission Type
Summary