Cleared Traditional

5MM MICROSCISSORS (K913870) - FDA 510(k) Clearance

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

K913870 · Endovations · General & Plastic Surgery device
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Sep 1991
Decision
18d
Days
Class 2
Risk

K913870 is an FDA 510(k) clearance for the 5MM MICROSCISSORS. Classified as Laparoscope, General & Plastic Surgery (product code GCJ), Class II - Special Controls.

Submitted by Endovations (Mechanicsburg, US). The FDA issued a Cleared decision on September 16, 1991 after a review of 18 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - 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 Endovations devices

Submission Details

510(k) Number K913870 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 29, 1991
Decision Date September 16, 1991
Days to Decision 18 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 115d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GCJ Laparoscope, General & Plastic Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 - GCJ Laparoscope, General & Plastic Surgery

All 354
Devices cleared under the same product code (GCJ) and FDA review panel - the closest regulatory comparables to K913870.
ENDOPATH DISPOSABLE ENDOSCOPIC MULTIFEED STAPLER
K913469 · Ethicon, Inc. · Sep 1991
ENDOSCOPE SUTURE & CARRIER
K912973 · United States Surgical, A Division of Tyco Healthc · Sep 1991
AUTO SUTURE ENDOSCOPIC FASCIA STAPLER
K912097 · United States Surgical, A Division of Tyco Healthc · Sep 1991
SUCTION/IRRIGATION DEVICE WITH HYDRO-DISSECTION
K911105 · United States Surgical, A Division of Tyco Healthc · Aug 1991
STERILE DISPOSABLE TROCAR-SLEEVE DEVICES
K862611 · United States Surgical, A Division of Tyco Healthc · Jul 1986