Definition
FITBONE systems use an implanted motor and receiver activated through an external control system. U.S. FDA records include clearances for FITBONE TAA and the FITBONE Transport and Lengthening System. A separate open recall identifies two units from specified 2024 lots of one trochanteric nail item; it is not a recall of every FITBONE system. Verify the exact model, catalog number, UDI or lot, current instructions, and country-specific status. [1][2][3]
Updated
Sources
- U.S. FDA - 510(k) Premarket Notification K203399: FITBONE TAAOfficial public sourceAccessed 2026-07-15
- U.S. FDA - 510(k) Premarket Notification K232169: FITBONE Transport and Lengthening SystemOfficial public sourceAccessed 2026-07-15
- U.S. FDA - Class 2 Device Recall: Fitbone Trochanteric Nail (Z-1977-2025)Official public sourceAccessed 2026-07-15
The open record identifies two units from specified lots and was last updated July 14, 2026.
Informational only. Not medical advice.