Last synced on 25 January 2026 at 3:41 am

SYNSTER PEDICLE SCREW SYSTEM SYNSTER PLUS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120353
510(k) Type
Traditional
Applicant
Bm Korea Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2012
Days to Decision
93 days
Submission Type
Summary

SYNSTER PEDICLE SCREW SYSTEM SYNSTER PLUS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120353
510(k) Type
Traditional
Applicant
Bm Korea Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2012
Days to Decision
93 days
Submission Type
Summary