Cleared Traditional

K051027 - STALIF TT

K051027 is an FDA 510(k) clearance for STALIF TT, manufactured by Surgicraft , Ltd.. The device is a Class 2 Orthopedic device with product code MQP cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K051027 · Surgicraft , Ltd. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2005
Decision
68d
Days
Class 2
Risk

K051027 is an FDA 510(k) clearance for the STALIF TT. Classified as Spinal Vertebral Body Replacement Device (product code MQP), Class II - Special Controls.

Submitted by Surgicraft , Ltd. (Chicago, US). The FDA issued a Cleared decision on June 29, 2005 after a review of 68 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3060 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Surgicraft , Ltd. devices

FDA 510(k) Submission Details - K051027

510(k) Number K051027 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 22, 2005
Decision Date June 29, 2005
Days to Decision 68 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 122d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQP Device Classification - Class 2, Special Controls

Product Code MQP Spinal Vertebral Body Replacement Device
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3060
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.

Regulatory Peers - MQP Spinal Vertebral Body Replacement Device

All 237
Devices cleared under the same product code (MQP) and FDA review panel - the closest regulatory comparables to K051027.
QUANTUM VERTEBRAL BODY REPLACEMENT
K050449 · Quantum Orthopedics, Inc. · Jul 2005
MC+ PARTIAL VBR
K043479 · Ldr Spine USA · Jun 2005
OPEN RADIOTRANSPARENT INTERSOMATIC IMPLANT (ROI)
K043349 · Ldr Spine USA · Jun 2005
TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1
K051196 · Implex Corp. · Jun 2005
CONSTRUX MINI PEEK VBR SYSTEM
K051246 · Blackstone Medical, Inc. · Jun 2005
BASIS VERTEBRAL BODY SPACER
K051105 · Medtronic Sofamor Danek · Jun 2005