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OSSIOfiber™ Compression Screws

Page Type
Cleared 510(K)
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)
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