Cleared Traditional

K060914 - TRIDENT ANCHOR

K060914 is an FDA 510(k) clearance for TRIDENT ANCHOR, manufactured by Johnson & Johnson Company. The device is a Class 2 Orthopedic device with product code HWC cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K060914 · Johnson & Johnson Company · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2006
Decision
66d
Days
Class 2
Risk

K060914 is an FDA 510(k) clearance for the TRIDENT ANCHOR. Classified as Screw, Fixation, Bone (product code HWC), Class II - Special Controls.

Submitted by Johnson & Johnson Company (Raynham, US). The FDA issued a Cleared decision on June 9, 2006 after a review of 66 days - a notably fast clearance cycle.

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: 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 Johnson & Johnson Company devices

FDA 510(k) Submission Details - K060914

510(k) Number K060914 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 2006
Decision Date June 09, 2006
Days to Decision 66 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
56d faster than avg
Panel avg: 122d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HWC Device Classification - Class 2, Special Controls

Product Code HWC Screw, Fixation, Bone
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 - HWC Screw, Fixation, Bone

All 943
Devices cleared under the same product code (HWC) and FDA review panel - the closest regulatory comparables to K060914.
MILAGRO INTERFERENCE SCREW
K060830 · Depuy Mitek, A Johnson & Johnson Company · Jun 2006
ULTRATINE TRANSBLEPH
K060248 · Coapt Systems, Inc. · Jun 2006
ULTRATINE FOREHEAD
K060249 · Coapt Systems, Inc. · Jun 2006
FASTIN RC ANCHOR
K060664 · Depuy Mitek · Jun 2006
MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR
K060693 · Arthrotek, Inc. · Jun 2006
ARTHREX BIO-COMPRESSION SCREW
K060478 · Arthrex, Inc. · May 2006