510(k) K173347

STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX by Centinel Spine, Inc. — Product Code MAX

K173347 is an FDA 510(k) premarket notification submitted by Centinel Spine, Inc. for the device "STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX". The FDA issued a decision of Substantially Equivalent on May 8, 2018. The device falls under product code MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), a Class II device regulated under 21 CFR 888.3080. Centinel Spine, Inc. has at least 10 other 510(k) clearances on record.