Last synced on 16 May 2025 at 11:05 pm

OSSIOfiber™ Compression Screws

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193660
510(k) Type
Traditional
Applicant
Ossio Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/30/2020
Days to Decision
213 days
Submission Type
Summary

OSSIOfiber™ Compression Screws

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193660
510(k) Type
Traditional
Applicant
Ossio Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/30/2020
Days to Decision
213 days
Submission Type
Summary