Cleared Traditional

K071477 - REVERTO 55 AND 37 SHAPE MEMORY STAPLES

K071477 is the FDA 510(k) clearance for REVERTO 55 AND 37 SHAPE MEMORY STAPLES by Core Essence Orthopaedics, LLC. It is a Class 2 Orthopedic device (product code JDR) cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K071477 · Core Essence Orthopaedics, LLC · Orthopedic device
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Optimized for regulatory review, auditing and printing
Aug 2007
Decision
78d
Days
Class 2
Risk

K071477 is an FDA 510(k) clearance for the REVERTO 55 AND 37 SHAPE MEMORY STAPLES. Classified as Staple, Fixation, Bone (product code JDR), Class II - Special Controls.

Submitted by Core Essence Orthopaedics, LLC (Yardley, US). The FDA issued a Cleared decision on August 15, 2007 after a review of 78 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.

View all Core Essence Orthopaedics, LLC devices

Submission Details

510(k) Number K071477 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 29, 2007
Decision Date August 15, 2007
Days to Decision 78 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
44d faster than avg
Panel avg: 122d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 98
Devices cleared under the same product code (JDR) and FDA review panel - the closest regulatory comparables to K071477.
CAIS STAPLE
K073281 · Depuy Mitek, A Johnson & Johnson Company · May 2008
ARTHREX COMPRESSION STAPLE
K080111 · Arthrex, Inc. · Feb 2008
BIOPRO MEMORY STAPLE, MODELS 18062-18073
K072298 · Biopro, Inc. · Oct 2007
MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD
K071257 · Depuy Mitek, A Johnson & Johnson Company · Jun 2007
BIOKNOTLESS AND LUPINE PLUS ANCHORS
K062170 · Depuy Mitek, A Johnson & Johnson Company · Aug 2006
BIOPRO MEMORY STAPLE
K061798 · Biopro, Inc. · Aug 2006