Last synced on 18 April 2025 at 11:05 pm

CRYSTALLINE BONE SCREW ENDO-OSSEOUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834364
510(k) Type
Traditional
Applicant
C.B.S. BIOTECHNICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1984
Days to Decision
131 days

CRYSTALLINE BONE SCREW ENDO-OSSEOUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K834364
510(k) Type
Traditional
Applicant
C.B.S. BIOTECHNICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1984
Days to Decision
131 days