Cleared Traditional

K142727 - CrossCLIP Implant System

K142727 is an FDA 510(k) clearance for CrossCLIP Implant System, manufactured by Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems. The device is a Class 2 Orthopedic device with product code JDR cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K142727 · Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems · Orthopedic device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 2014
Decision
31d
Days
Class 2
Risk

K142727 is an FDA 510(k) clearance for the CrossCLIP Implant System. Classified as Staple, Fixation, Bone (product code JDR), Class II - Special Controls.

Submitted by Orthodiscovery Group, LLC(D.B.A. Crossroads Extremity Systems (Collierville, US). The FDA issued a Cleared decision on October 24, 2014 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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.

FDA 510(k) Submission Details - K142727

510(k) Number K142727 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 2014
Decision Date October 24, 2014
Days to Decision 31 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
91d faster than avg
Panel avg: 122d · This submission: 31d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDR Device Classification - Class 2, Special Controls

Product Code JDR Staple, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 - JDR Staple, Fixation, Bone

All 222
Devices cleared under the same product code (JDR) and FDA review panel - the closest regulatory comparables to K142727.
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COMPRESSYN STAPLE
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