Nexa Orthopedics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K072710NEXFIX COMPRESSION PINNovember 8, 2007
K071147NEXA ORTHOPEDICS TOTAL SHOULDER SYSTEMJuly 20, 2007
K070688NEXFIX COMPRESSION STAPLEMay 18, 2007
K060386NEXA CARPO METACARPAL IMPLANTMay 10, 2006
K060071NEXA COMPRESSION SCREWJanuary 26, 2006
K053408NEXA BONE PLATE AND SCREW SYSTEMDecember 22, 2005
K053394NEXA BONE SCREW SYSTEMDecember 14, 2005
K051740TAPERED COMPRESSION PINSeptember 6, 2005
K051406OSTEOCURE RESORBABLE BEAD KITAugust 1, 2005
K033046SUBTALAR PEG IMPLANTDecember 23, 2003
K032902SUBTALAR ARTHRORISIS IMPLANTDecember 15, 2003
K023531LESSER METATARSAL PHALANGEAL JOINT IMPLANTJanuary 17, 2003
K023562MODIFICATION TO CLASSIC GREAT TOE IMPLANTNovember 13, 2002
K023086CLASSIC GREAT TOE IMPLANTOctober 4, 2002
K981194FUTURA BIOMEDICAL FLEXIBLE GREAT TOE IMPLANTJune 30, 1998
K971047FUTURA BIOMEDICAL METAL HEMI TOE IMPLANTJune 20, 1997