Last synced on 14 November 2025 at 11:06 pm

Peekplus® Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K173864
510(k) Type
Traditional
Applicant
Vallum Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2018
Days to Decision
194 days
Submission Type
Summary

Peekplus® Interbody Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K173864
510(k) Type
Traditional
Applicant
Vallum Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2018
Days to Decision
194 days
Submission Type
Summary