Cleared Traditional

K100724 - OSSEOTITE II MODEL XIFOSSXXX

K100724 is an FDA 510(k) clearance for OSSEOTITE II MODEL XIFOSSXXX, manufactured by Biomet 3i, Inc.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 382-day FDA review.

K100724 · Biomet 3i, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Apr 2011
Decision
382d
Days
Class 2
Risk

K100724 is an FDA 510(k) clearance for the OSSEOTITE II MODEL XIFOSSXXX. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Biomet 3i, Inc. (Palm Beach Gardens, US). The FDA issued a Cleared decision on April 1, 2011 after a review of 382 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - the FDA dental 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K100724

510(k) Number K100724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2010
Decision Date April 01, 2011
Days to Decision 382 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
254d slower than avg
Panel avg: 128d · This submission: 382d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
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 Dental devices follow this clearance model.

Regulatory Peers - DZE Implant, Endosseous, Root-form

All 1483
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K100724.
INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM
K103194 · Intra-Lock International, Inc. · Apr 2011
BLUE SKY BIO DENTAL IMPLANT SYSTEM
K102034 · Blue Sky Bio, LLC · Apr 2011
STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,
K101201 · Kat Implants, LLC · Apr 2011
APOLONIA LASER IMPLANT SYSTEM
K102635 · Csm Implant Co., Ltd. · Mar 2011
ANTHOFIT OI, ANTHOFIT HE, OSSFIT AND AXIOM
K101913 · Anthogyr Sas · Mar 2011
ET III SA ULTRA WIDE SYSTEM
K103537 · Hiossen, Inc. · Mar 2011
K100724 · OSSEOTITE II MODEL XIFOSSXXX
Download PDF FDA Summary Biomet 3i, Inc.