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OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable Fixation Nail

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231272
510(k) Type
Traditional
Applicant
OSSIO Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
213 days
Submission Type
Summary

OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable Fixation Nail

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231272
510(k) Type
Traditional
Applicant
OSSIO Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/1/2023
Days to Decision
213 days
Submission Type
Summary