Cleared Traditional

K896554 - GUT SUTURES

K896554 is an FDA 510(k) clearance for GUT SUTURES, manufactured by Look, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GAL cleared through the Traditional 510(k) pathway after a 195-day FDA review.

K896554 · Look, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1990
Decision
195d
Days
Class 2
Risk

K896554 is an FDA 510(k) clearance for the GUT SUTURES. Classified as Suture, Absorbable, Natural (product code GAL), Class II - Special Controls.

Submitted by Look, Inc. (Washington, US). The FDA issued a Cleared decision on May 31, 1990 after a review of 195 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4830 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Look, Inc. devices

FDA 510(k) Submission Details - K896554

510(k) Number K896554 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received November 17, 1989
Decision Date May 31, 1990
Days to Decision 195 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
80d slower than avg
Panel avg: 115d · This submission: 195d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAL Device Classification - Class 2, Special Controls

Product Code GAL Suture, Absorbable, Natural
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4830
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 - GAL Suture, Absorbable, Natural

All 17
Devices cleared under the same product code (GAL) and FDA review panel - the closest regulatory comparables to K896554.
AUTO SUTURE(R) MODIFIED ENDOSCOPIC LIGATING LOOP
K904588 · United States Surgical, A Division of Tyco Healthc · Dec 1990
PLAIN AND CHROMIC GUT SUTURE
K903624 · Look, Inc. · Sep 1990
ENDOSCOPIC HEMOSTATIC LIGATING LOOP
K902731 · United States Surgical, A Division of Tyco Healthc · Sep 1990
ABSORBABLE SURGICAL GUT SUTURE*
K885018 · United States Surgical, A Division of Tyco Healthc · Aug 1989