510(k) K120291

OP SPINE SYSTEM by OrthoPediatrics Corp. — Product Code OSH

K120291 is an FDA 510(k) premarket notification submitted by OrthoPediatrics Corp. for the device "OP SPINE SYSTEM". The FDA issued a decision of SESU on April 16, 2012. The device falls under product code OSH (Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis), a Class II device regulated under 21 CFR 888.3070. OrthoPediatrics Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESU ()
Decision Date
April 16, 2012
Date Received
January 31, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
Device Class
Class II
Regulation Number
888.3070
Review Panel
OR
Submission Type

Intended to stabilize the thoracolumbar spine as an adjunct to fusion using allograft and/or autograft to treat adolescent idiopathic scoliosis.