Cleared Traditional

K911905 - DEKNATEL MICROFLEX OPHTHAL POLY SUTURE

K911905 is an FDA 510(k) clearance for DEKNATEL MICROFLEX OPHTHAL POLY SUTURE, manufactured by Deknatel, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GAW cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K911905 · Deknatel, Inc. · General & Plastic Surgery device
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Jul 1991
Decision
74d
Days
Class 2
Risk

K911905 is an FDA 510(k) clearance for the DEKNATEL(R) MICROFLEX OPHTHAL POLY SUTURE,MODIFIED. Classified as Suture, Nonabsorbable, Synthetic, Polypropylene (product code GAW), Class II - Special Controls.

Submitted by Deknatel, Inc. (San Jose-Heredia, CR). The FDA issued a Cleared decision on July 2, 1991 after a review of 74 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5010 - 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 Deknatel, Inc. devices

FDA 510(k) Submission Details - K911905

510(k) Number K911905 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 19, 1991
Decision Date July 02, 1991
Days to Decision 74 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
41d faster than avg
Panel avg: 115d · This submission: 74d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAW Device Classification - Class 2, Special Controls

Product Code GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5010
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 - GAW Suture, Nonabsorbable, Synthetic, Polypropylene

All 28
Devices cleared under the same product code (GAW) and FDA review panel - the closest regulatory comparables to K911905.
REVISED LABELING FOR POLYPROPYLENE SUTURE
K926588 · Look, Inc. · Dec 1993
SURGILENE POLYPROPYLENE SUTURE
K930587 · Davis & Geck, Inc. · Dec 1993
SYNTHETIC ABSORBABLE SUTURE, UNDYED
K920437 · Ethicon, Inc. · Jul 1992
DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE
K903643 · Deknatel, Inc. · Dec 1990
POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES
K903584 · Look, Inc. · Oct 1990
NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE*
K902872 · United States Surgical, A Division of Tyco Healthc · Sep 1990