Cleared Traditional

K121713 - PMT BONE SCREWS

K121713 is an FDA 510(k) clearance for PMT BONE SCREWS, manufactured by Providence Medical Technology, Inc.. The device is a Class 2 Orthopedic device with product code HWC cleared through the Traditional 510(k) pathway after a 108-day FDA review.

K121713 · Providence Medical Technology, Inc. · Orthopedic device
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Sep 2012
Decision
108d
Days
Class 2
Risk

K121713 is an FDA 510(k) clearance for the PMT BONE SCREWS. Classified as Screw, Fixation, Bone (product code HWC), Class II - Special Controls.

Submitted by Providence Medical Technology, Inc. (Lafayette, US). The FDA issued a Cleared decision on September 27, 2012 after a review of 108 days - within the typical 510(k) review window.

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: 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.

View all Providence Medical Technology, Inc. devices

FDA 510(k) Submission Details - K121713

510(k) Number K121713 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 11, 2012
Decision Date September 27, 2012
Days to Decision 108 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d faster than avg
Panel avg: 122d · This submission: 108d
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 681
Devices cleared under the same product code (HWC) and FDA review panel - the closest regulatory comparables to K121713.
ACUMED CANNULATED SCREW SYSTEM
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K121349 · Extremity Medical, LLC · Jul 2012
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K121417 · Extremity Medical, LLC · Jul 2012
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K120645 · Wrightmedicaltechnologyinc · Apr 2012