Cleared Traditional

K992616 - SDB CERCLAGE SYSTEM

K992616 is an FDA 510(k) clearance for SDB CERCLAGE SYSTEM, manufactured by Pioneer Surgical Technology. The device is a Class 2 Orthopedic device with product code JDQ cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K992616 · Pioneer Surgical Technology · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1999
Decision
84d
Days
Class 2
Risk

K992616 is an FDA 510(k) clearance for the SDB CERCLAGE SYSTEM. Classified as Cerclage, Fixation (product code JDQ), Class II - Special Controls.

Submitted by Pioneer Surgical Technology (Marquette, US). The FDA issued a Cleared decision on October 27, 1999 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3010 - 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 Pioneer Surgical Technology devices

FDA 510(k) Submission Details - K992616

510(k) Number K992616 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1999
Decision Date October 27, 1999
Days to Decision 84 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
38d faster than avg
Panel avg: 122d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDQ Device Classification - Class 2, Special Controls

Product Code JDQ Cerclage, Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3010
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 - JDQ Cerclage, Fixation

All 110
Devices cleared under the same product code (JDQ) and FDA review panel - the closest regulatory comparables to K992616.
WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
K993903 · Whiteside Biomechanics, Inc. · Feb 2000
PIONEER SILICOAT STERNAL CABLE
K993286 · Pioneer Surgical Technology · Nov 1999
SYNTHES CERCLAGE POSITIONING PIN
K992891 · Synthes (Usa) · Nov 1999
DALL-MILES CABLE GRIP (A-GRIP)
K984432 · Howmedica Osteonics Corp. · Feb 1999
METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM
K983976 · Metagen, LLC · Dec 1998
BMP CABLE SYSTEM
K982545 · Biomet, Inc. · Oct 1998