510(k) K172183
K172183 is an FDA 510(k) premarket notification submitted by Orthofix Srl for the device "Guided Growth Plate System Plus". The FDA issued a decision of Substantially Equivalent on January 9, 2018. The device falls under product code OBT (Plate, Bone, Growth Control, Pediatric, Epiphysiodesis), a Class II device regulated under 21 CFR 888.3030. Orthofix Srl has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 9, 2018
- Date Received
- July 19, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plate, Bone, Growth Control, Pediatric, Epiphysiodesis
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
Intended to redirect the angle of growth of long bone(s) only in pediatric patients. Indicated for temporary or permanent epiphysiodesis. For gradually correcting angular deformities of long bones in pediatric patients with an open physis. Specific conditions/diseases for which the device will be indicated include valgus, varus, or flexion extension deformities of the knee (femur and/or tibia); valgus, varus or plantar flexion deformities of the ankle, valgus or varus deformities of the elbow, as well as radial or ulnar deviation, flexion or extension deformities of the wrist (radius). The device may be removed when growth has equalized or the growth plate has fused.