Last synced on 14 November 2025 at 11:06 pm

REESE ARTHRODESIS SCREW

Page Type
Cleared 510(K)
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)
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