Nexa Orthopedics, Inc.
Nexa Orthopedics, Inc. appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 8, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 16
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K072710 | NEXFIX COMPRESSION PIN | November 8, 2007 |
| K071147 | NEXA ORTHOPEDICS TOTAL SHOULDER SYSTEM | July 20, 2007 |
| K070688 | NEXFIX COMPRESSION STAPLE | May 18, 2007 |
| K060386 | NEXA CARPO METACARPAL IMPLANT | May 10, 2006 |
| K060071 | NEXA COMPRESSION SCREW | January 26, 2006 |
| K053408 | NEXA BONE PLATE AND SCREW SYSTEM | December 22, 2005 |
| K053394 | NEXA BONE SCREW SYSTEM | December 14, 2005 |
| K051740 | TAPERED COMPRESSION PIN | September 6, 2005 |
| K051406 | OSTEOCURE RESORBABLE BEAD KIT | August 1, 2005 |
| K033046 | SUBTALAR PEG IMPLANT | December 23, 2003 |
| K032902 | SUBTALAR ARTHRORISIS IMPLANT | December 15, 2003 |
| K023531 | LESSER METATARSAL PHALANGEAL JOINT IMPLANT | January 17, 2003 |
| K023562 | MODIFICATION TO CLASSIC GREAT TOE IMPLANT | November 13, 2002 |
| K023086 | CLASSIC GREAT TOE IMPLANT | October 4, 2002 |
| K981194 | FUTURA BIOMEDICAL FLEXIBLE GREAT TOE IMPLANT | June 30, 1998 |
| K971047 | FUTURA BIOMEDICAL METAL HEMI TOE IMPLANT | June 20, 1997 |