Last synced on 30 May 2025 at 11:05 pm

SYNTHES 7.0/7.3 MM CANNULATED SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962011
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/5/1996
Days to Decision
74 days

SYNTHES 7.0/7.3 MM CANNULATED SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962011
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/5/1996
Days to Decision
74 days