Wishbone Medical, Inc.
Wishbone Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2023, with 3 FDA device recalls on record.
Top product codes for Wishbone Medical, Inc.
FDA recalls by Wishbone Medical, Inc.
- Z-1808-2024 — WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
- Z-1102-2023 — WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS 10-702-095115-0 Short 10-702-115150-0 Medium 10-702-140200 Long 10-702-190300-0
- Z-1794-2021 — WishBone Medical Plate and Screw System - Screw, Fixation, Bone, Washer, Bolt Nut. Part Number: PK-SMC0635NL-TI-US, PK-SMC0635NR-TI-US, PK-SMC0835NSL-TI-US, PK-SMC0835NSR-TI-US
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Wishbone Medical, Inc.
- K231461 — Smart Correction System (HA Half Pins)
- K230527 — WishBone Medical Plate and Screw System
- K221366 — Smart Correction System Rings and Compatible HA-Coated Half Pins
- K213489 — Wishbone Medical Plate and Screw System: 3.0mm Screws and 7-Hole Straight Fibula Plate
- K203467 — WishBone Medical Plate and Screw System
- K193368 — Smart Correction System
- K180736 — WishBone Medical Plate and Screw System
- K173013 — WishBone K-Wire System
Data sourced from openFDA. This site is unofficial and independent of the FDA.