Cleared Abbreviated

K072415 - STALIF (TM) C

K072415 is an FDA 510(k) clearance for STALIF (TM) C, manufactured by Surgicraft , Ltd.. The device is a Class 2 Orthopedic device with product code OVE cleared through the Abbreviated 510(k) pathway after a 150-day FDA review.

K072415 · Surgicraft , Ltd. · Orthopedic device
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Jan 2008
Decision
150d
Days
Class 2
Risk

K072415 is an FDA 510(k) clearance for the STALIF (TM) C. Classified as Intervertebral Fusion Device With Integrated Fixation, Cervical (product code OVE), Class II - Special Controls.

Submitted by Surgicraft , Ltd. (Douglassville, US). The FDA issued a Cleared decision on January 25, 2008 after a review of 150 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - the FDA orthopedic device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Surgicraft , Ltd. devices

FDA 510(k) Submission Details - K072415

510(k) Number K072415 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 28, 2007
Decision Date January 25, 2008
Days to Decision 150 days
Submission Type Abbreviated
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
28d slower than avg
Panel avg: 122d · This submission: 150d
Pathway characteristics
Standards-based clearance path.

OVE Device Classification - Class 2, Special Controls

Product Code OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Cervical Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft With Or Without Supplemental Fixation.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.