NDF — Plate, Fixation, Bone, Non-Spinal, Metallic Class II
FDA Device Classification
Classification Details
- Product Code
- NDF
- Device Class
- Class II
- Regulation Number
- 888.3030
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K051642 | i.t.s. implantat-technologie-systeme | FR.O.H. CALCANEUS REPAIR SYSTEM | August 22, 2005 |
| K021749 | ebi, l.p | EBI DYNAFIX VS OSTEOTOMY SYSTEM | August 12, 2002 |
| K010551 | ebi, l.p | EBI DYNAFIX VS OSTEOTOMY SYSTEM | May 17, 2001 |