Last synced on 24 May 2024 at 11:04 pm

ORTHOFIX SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113650
510(k) Type
Traditional
Applicant
BONAFIX SURGICAL AND DENTAL IMPLANTS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2012
Days to Decision
296 days
Submission Type
Summary

ORTHOFIX SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113650
510(k) Type
Traditional
Applicant
BONAFIX SURGICAL AND DENTAL IMPLANTS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2012
Days to Decision
296 days
Submission Type
Summary