Home › Device types › NDF
Plate, Fixation, Bone, Non-Spinal, Metallic
FDA product code NDF · Class 2 · Orthopedic
47
Registered devices
8
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
DYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCPolyLock SmallBone — FUSION ORTHOPEDICS, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-10-11 | Zimmer, Inc. | Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this r |
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