Cleared Traditional

K103623 - NEWDEAL INTERPHALANGEAL IMPLANT

K103623 is an FDA 510(k) clearance for NEWDEAL INTERPHALANGEAL IMPLANT, manufactured by Newdeal Sas. The device is a Class 2 Orthopedic device with product code HTY cleared through the Traditional 510(k) pathway after a 466-day FDA review.

K103623 · Newdeal Sas · Orthopedic device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2012
Decision
466d
Days
Class 2
Risk

K103623 is an FDA 510(k) clearance for the NEWDEAL INTERPHALANGEAL IMPLANT. Classified as Pin, Fixation, Smooth (product code HTY), Class II - Special Controls.

Submitted by Newdeal Sas (Parc Technologique De La Prte, FR). The FDA issued a Cleared decision on March 20, 2012 after a review of 466 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

FDA 510(k) Submission Details - K103623

510(k) Number K103623 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 2010
Decision Date March 20, 2012
Days to Decision 466 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
344d slower than avg
Panel avg: 122d · This submission: 466d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HTY Device Classification - Class 2, Special Controls

Product Code HTY Pin, Fixation, Smooth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
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 - HTY Pin, Fixation, Smooth

All 198
Devices cleared under the same product code (HTY) and FDA review panel - the closest regulatory comparables to K103623.
TRILLIANT SURGICAL K-WIRES
K121008 · Trilliant Surgical, Ltd. · Jun 2012
APEX KIRSCHNER WIRES AND STEINMANN PINS
K121004 · Apex Tools & Orthopedics Co. · Apr 2012
INTRAOSSEOUS FIXATION SYSTEM
K120165 · Orthohelix Surgical Designs, Inc. · Apr 2012
ACL TIGHTROPE,ACL TIGHTROPE DUUBLE BUNDLE
K112990 · Arthrex, Inc. · Dec 2011
ARROW-LOK DIGITAL SYSTEM
K112675 · Arrowhead Medical Device Technologies, LLC · Dec 2011
MEMOMETAL INTRA-MEDULLARY BONE FASTENER
K112197 · Memometal Technologies · Nov 2011
K103623 · NEWDEAL INTERPHALANGEAL IMPLANT
Download PDF FDA Summary Newdeal Sas