510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K861876Substantially Equivalent

Cranio Blades and Wire Pass Drill

New England Surgical Instrument Corp., Rockland MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861876 is the FDA 510(k) clearance record for CRANIO BLADES AND WIRE PASS DRILL, a class I device, cleared for New England Surgical Instrument Corp. on under FDA product code GFA (Blade, Saw, General & Plastic Surgery, Surgical). FDA records list 18 510(k) clearances for New England Surgical Instrument Corp., from to . As of , FDA records show no recalls naming K861876.

Clearance record

Decision date
Received
(15 days to decision)
Product code
GFA Blade, Saw, General & Plastic Surgery, Surgical
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
New England Surgical Instrument Corp. P.O. Box 35, Rockland MA
Third party review
No

Clearances, product code GFA

Trailing 12 months

FDA records hold no clearances under product code GFA in the trailing twelve months.

FDA records show no clearances under product code GFA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GFA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260