Cleared Traditional

K812160 - MICROSURGICAL BLADE

K812160 is the FDA 510(k) clearance for MICROSURGICAL BLADE by Vxtra Corp.. It is a Class 1 General & Plastic Surgery device (product code GES) cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K812160 · Vxtra Corp. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1981
Decision
33d
Days
Class 1
Risk

K812160 is an FDA 510(k) clearance for the MICROSURGICAL BLADE. Classified as Blade, Scalpel (product code GES), Class I - General Controls.

Submitted by Vxtra Corp. (Mchenry, US). The FDA issued a Cleared decision on August 31, 1981 after a review of 33 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - 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 Vxtra Corp. devices

Submission Details

510(k) Number K812160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 29, 1981
Decision Date August 31, 1981
Days to Decision 33 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
82d faster than avg
Panel avg: 115d · This submission: 33d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GES Blade, Scalpel
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GES Blade, Scalpel

All 10
Devices cleared under the same product code (GES) and FDA review panel - the closest regulatory comparables to K812160.
H.R. JAKOBI SURG. INSTRUMENTS #11 27/37
K834182 · Imm Enterprises , Ltd. · Jan 1984
JAKOBI SURG. INSTRUMENTS #1 19/10/26
K834194 · Imm Enterprises , Ltd. · Jan 1984
JAKOBI SURG. INSTRUMENTS #11 11/13/14
K834195 · Imm Enterprises , Ltd. · Jan 1984
BLADE, 20 ANGLE/MICRO BLADE HOLDER
K781716 · Edward Weck, Inc. · Oct 1978
SURGICAL BLADES
K761322 · Richard-Allan Medical Ind., Inc. · Jan 1977