Product code KWO— Orthopedic
SWANSON TITANIUM CARPAL SCAPHOID IMPLANT
- Classification name
- Prosthesis, Wrist, Carpal Scaphoid
- Device class
- Class 2
- Regulation
- 21 CFR 888.3760
- Advisory panel
- Orthopedic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KWO
FDA has cleared device under product code KWO, all in 1987, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code KWO
Recent clearances under product code KWO
Data sourced from openFDA. This site is unofficial and independent of the FDA.