Last synced on 18 July 2025 at 11:06 pm

2.4MM CORTEX SCREW, SELF-TAPPING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002271
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2000
Days to Decision
30 days
Submission Type
Summary

2.4MM CORTEX SCREW, SELF-TAPPING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002271
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2000
Days to Decision
30 days
Submission Type
Summary