Last synced on 23 May 2025 at 11:06 pm

REESE ARTHRODESIS SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860323
510(k) Type
Traditional
Applicant
OSTEOTOMY GUIDE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1986
Days to Decision
21 days

REESE ARTHRODESIS SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860323
510(k) Type
Traditional
Applicant
OSTEOTOMY GUIDE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1986
Days to Decision
21 days