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Mega Plus Spine System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173180
510(k) Type
Traditional
Applicant
BK MEDITECH Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/15/2018
Days to Decision
167 days
Submission Type
Summary

Mega Plus Spine System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173180
510(k) Type
Traditional
Applicant
BK MEDITECH Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/15/2018
Days to Decision
167 days
Submission Type
Summary