Last synced on 13 June 2025 at 11:06 pm

Meridian Interbody System; WaveForm A Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233694
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
56 days
Submission Type
Summary

Meridian Interbody System; WaveForm A Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233694
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2024
Days to Decision
56 days
Submission Type
Summary