Cleared Traditional

K861922 - TITANIUM HEMOSTATIC CLIPS

K861922 is an FDA 510(k) clearance for TITANIUM HEMOSTATIC CLIPS, manufactured by Pilling Co.. The device is a Class 2 General & Plastic Surgery device with product code FZP cleared through the Traditional 510(k) pathway after a 25-day FDA review.

K861922 · Pilling Co. · General & Plastic Surgery device
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Jun 1986
Decision
25d
Days
Class 2
Risk

K861922 is an FDA 510(k) clearance for the TITANIUM HEMOSTATIC CLIPS. Classified as Clip, Implantable (product code FZP), Class II - Special Controls.

Submitted by Pilling Co. (Fort Washington, US). The FDA issued a Cleared decision on June 13, 1986 after a review of 25 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4300 - 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 Pilling Co. devices

FDA 510(k) Submission Details - K861922

510(k) Number K861922 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 19, 1986
Decision Date June 13, 1986
Days to Decision 25 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
90d faster than avg
Panel avg: 115d · This submission: 25d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FZP Device Classification - Class 2, Special Controls

Product Code FZP Clip, Implantable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4300
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 - FZP Clip, Implantable

All 108
Devices cleared under the same product code (FZP) and FDA review panel - the closest regulatory comparables to K861922.
VICRYL* POLYGLACTIN 730 ABSORBABLE STAPLES/STAPLER
K864350 · Ethicon, Inc. · Dec 1986
LIGACLIP 20/20* MULTIPLE CLIP APPLIER
K864102 · Ethicon, Inc. · Nov 1986
REFLEX(TM) CLIP APPLIER
K862404 · Richard-Allan Medical Ind., Inc. · Jul 1986
V. MUELLER VITAL CLIP-HEMOSTATIC CLIP
K861471 · American V. Mueller · Jun 1986
AUTO SUTURE TITANIUM HEMOSTATIC CLIP
K853650 · United States Surgical, A Division of Tyco Healthc · Sep 1985
AUTO/MANUAL TITANIUM HEMOCLIP LIGATING CLIP 527200
K851251 · Edward Weck, Inc. · Jul 1985