Cleared Traditional

AUTO SUTURE(R) THIN TISSUE GIA(TM) SURG STAPLER (K913211) - FDA 510(k) Clearance

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K913211 · United States Surgical, A Division of Tyco Healthc · General & Plastic Surgery device
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Sep 1991
Decision
68d
Days
Class 2
Risk

K913211 is an FDA 510(k) clearance for the AUTO SUTURE(R) THIN TISSUE GIA(TM) SURG STAPLER. Classified as Staple, Implantable (product code GDW), Class II - Special Controls.

Submitted by United States Surgical, A Division of Tyco Healthc (Norwalk, US). The FDA issued a Cleared decision on September 25, 1991 after a review of 68 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4750 - the FDA general and plastic surgery device 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 K913211 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 1991
Decision Date September 25, 1991
Days to Decision 68 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 115d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GDW Staple, Implantable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4750
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GDW Staple, Implantable

All 106
Devices cleared under the same product code (GDW) and FDA review panel - the closest regulatory comparables to K913211.
AUTO SUTURE(R) POWERED ENDOSCOPIC GIA(TM) STAPLER
K913802 · United States Surgical, A Division of Tyco Healthc · Oct 1991
AUTO SUTURE(R) POWERED ENDOSCOPIC TA(R) STAPLER
K913832 · United States Surgical, A Division of Tyco Healthc · Oct 1991
AUTO SUTURE TITANIUM SKIN AND FASCIA STAPLES
K914130 · United States Surgical, A Division of Tyco Healthc · Oct 1991
IMPLANTABLE METAL STAPLES
K913139 · Ethicon, Inc. · Sep 1991
AUTO SUTURE ENDOSCOPIC TA SURGICAL STAPLER
K910192 · United States Surgical, A Division of Tyco Healthc · Feb 1991
AUTO SUTURE(R) TA PREMIUM(TM) UROLOGY STAPLER
K905106 · United States Surgical, A Division of Tyco Healthc · Jan 1991