Cleared Traditional

K123926 - METASURG NITINOL STAPLE IMPLANT

K123926 is an FDA 510(k) clearance for METASURG NITINOL STAPLE IMPLANT, manufactured by Metasurg. The device is a Class 2 Orthopedic device with product code JDR cleared through the Traditional 510(k) pathway after a 134-day FDA review.

K123926 · Metasurg · Orthopedic device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 2013
Decision
134d
Days
Class 2
Risk

K123926 is an FDA 510(k) clearance for the METASURG NITINOL STAPLE IMPLANT. Classified as Staple, Fixation, Bone (product code JDR), Class II - Special Controls.

Submitted by Metasurg (Houston, US). The FDA issued a Cleared decision on May 3, 2013 after a review of 134 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K123926

510(k) Number K123926 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 20, 2012
Decision Date May 03, 2013
Days to Decision 134 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
12d slower than avg
Panel avg: 122d · This submission: 134d
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 K123926.
ORTHOHELIX STAPLE SYSTEM
K130832 · Orthohelix Surgical Designs, Inc. · Aug 2013
FUSEFORCE IMPLANT SYSTEM
K124045 · Solana Surgical, LLC · Jul 2013
SPEED SHIFT
K124022 · Biomedical Enterprises, Inc. · May 2013
MEMORY METAL STAPLES, EASYCLIP
K122113 · Stryker Corp. · Mar 2013
COMPRESSYN STAPLE
K122871 · Dallen Medical, Inc. · Feb 2013
SUPER STAPLE(TM) CLASSIC
K123363 · Metric Medical Devices, Inc. · Jan 2013