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RemeOs™ Screw LAG Solid

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220030
510(k) Type
Direct
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Deleted
Decision Date
3/29/2023
Days to Decision
329 days

RemeOs™ Screw LAG Solid

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN220030
510(k) Type
Direct
Applicant
Bioretec , Ltd.
Country
Finland
FDA Decision
Deleted
Decision Date
3/29/2023
Days to Decision
329 days