Cleared Traditional

K893707 - AUTO SUTURE SURGIPORT DEPTH GUIDE AND S...

K893707 is the FDA 510(k) clearance for AUTO SUTURE SURGIPORT DEPTH GUIDE AND S... by United States Surgical, A Division of Tyco Healthc. It is a Class 2 Cardiovascular device (product code DRC) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K893707 · United States Surgical, A Division of Tyco Healthc · Cardiovascular device
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Jun 1989
Decision
28d
Days
Class 2
Risk

K893707 is an FDA 510(k) clearance for the AUTO SUTURE SURGIPORT DEPTH GUIDE AND SKIRT. Classified as Trocar (product code DRC), Class II - Special Controls.

Submitted by United States Surgical, A Division of Tyco Healthc (Norwalk, US). The FDA issued a Cleared decision on June 15, 1989 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1390 - the FDA cardiovascular device oversight 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 United States Surgical, A Division of Tyco Healthc devices

Submission Details

510(k) Number K893707 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 1989
Decision Date June 15, 1989
Days to Decision 28 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 125d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRC Trocar
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1390
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DRC Trocar

All 29
Devices cleared under the same product code (DRC) and FDA review panel - the closest regulatory comparables to K893707.
LAPAROSCOPIC TROCAR
K911483 · United States Endoscopy Group, Inc. · Jul 1991
SELDINGER SINGLE WALL
K895454 · Advance Medical Designs, Inc. · Nov 1989
SELDINGER PERCUTANEOUS 2 PC NEEDLES
K895455 · Advance Medical Designs, Inc. · Nov 1989
DISPOSABLE ANGIOGRAPHY NEEDLES
K890209 · E-Z-Em, Inc. · May 1989
NAMIC COURNAND STYLE INTRODUCER NEEDLE
K871377 · North American Instrument Corp. · May 1987
NAMIC SELDINGER INTRODUCER NEEDLE
K871378 · North American Instrument Corp. · May 1987