Cleared Traditional

K971654 - OSTEO COMPRESSION HIP SCREW SYSTEM

K971654 is an FDA 510(k) clearance for OSTEO COMPRESSION HIP SCREW SYSTEM, manufactured by Osteonics Corp.. The device is a Class 2 Orthopedic device with product code HWC cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K971654 · Osteonics Corp. · Orthopedic device
Download Printable Device Report (PDF)
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Jul 1997
Decision
64d
Days
Class 2
Risk

K971654 is an FDA 510(k) clearance for the OSTEO COMPRESSION HIP SCREW SYSTEM. Classified as Screw, Fixation, Bone (product code HWC), Class II - Special Controls.

Submitted by Osteonics Corp. (Allendale, US). The FDA issued a Cleared decision on July 9, 1997 after a review of 64 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 Osteonics Corp. devices

FDA 510(k) Submission Details - K971654

510(k) Number K971654 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1997
Decision Date July 09, 1997
Days to Decision 64 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
58d faster than avg
Panel avg: 122d · This submission: 64d
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 979
Devices cleared under the same product code (HWC) and FDA review panel - the closest regulatory comparables to K971654.
34MM SCARF THREAD-HEAD(TM) SCREW
K971068 · Landos, Inc. · Jul 1997
TWIST-OFF (TM) SCREW
K971069 · Landos, Inc. · Jul 1997
SCARF THREAD-HEAD (TM) HEAD SCREW
K971070 · Landos, Inc. · Jul 1997
OSTEO SMALL AND MINI BONE SCREWS
K971778 · Osteonics Corp. · Jun 1997
DEPUY LOW PROFILE BONE SCREW
K970929 · Depuy, Inc. · Jun 1997
TITANIUM ALLOY BONE SCREWS
K970549 · Aesculap, Inc. · Apr 1997