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510(k) K171151

ACRON™ TLIF System by Spinemed Ges.M.B.H — Product Code MAX

K171151 is an FDA 510(k) premarket notification submitted by Spinemed Ges.M.B.H for the device "ACRON™ TLIF System". The FDA issued a decision of Substantially Equivalent on Apr 27, 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.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 27, 2018
Date Received
Apr 20, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class
Class II
Regulation Number
888.3080
Review Panel
OR
Submission Type
510(k)

Intended to stabilize spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.

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FDA data resources