Last synced on 23 September 2022 at 11:05 pm

SB ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140600
510(k) Type
Traditional
Applicant
OSSTEM IMPLANT CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2014
Days to Decision
164 days
Submission Type
Summary

SB ANCHOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140600
510(k) Type
Traditional
Applicant
OSSTEM IMPLANT CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2014
Days to Decision
164 days
Submission Type
Summary