Home › Device types › NDH
Nail, Fixation, Bone, Metallic
FDA product code NDH · Class 2 · Orthopedic
52
Registered devices
3
Adverse events
3
Recalls
0
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, LLCFlow-Screw™ — Flow-FXDYNAFIX 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, LLCFlow-Nail™ — Flow-FXDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLCFlow-Nail™ — Flow-FXDYNAFIX VS OSTEOTOMY SYSTEM — Biomet Orthopedics, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-11-22 | Stryker Howmedica Osteonics Corp. | The Gamma Nail may have been manufactured with an incorrect lag screw hole angulation. Catalog number 3225-0360S, lot code K949396 was manufactured with a lag s |
| 2004-09-07 | Stryker Howmedica Osteonics Corp. | Stryker became aware that Catalog number 1594-1130S, Lot Code K559623 was manufactured with a lag screw hold angulation of 135 degrees rather than 130 degrees. |
| 2002-12-11 | Disc Orthopaedic Technologies Inc | The Fixion Interlocking Proximal Femoral Hip Pegs are defective due to possible tension failure. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
