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/ Osteotomy Guide Co.
Osteotomy Guide Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K861576
SHORTENING OSTEOTOMY GUIDE
May 12, 1986
K860323
REESE ARTHRODESIS SCREW
February 19, 1986
K841470
REESE OSTEOTOMY GUIDE SYS
May 23, 1984