Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K896946Substantially Equivalent

Coated Novafil, Polybutester, Mesh

American Cyanamid Co., Danbury CT / Traditional, Substantially Equivalent

K896946 is the FDA 510(k) clearance record for COATED NOVAFIL, POLYBUTESTER, MESH, a class II device, cleared for American Cyanamid Co. on under FDA product code FTM (Mesh, Surgical). FDA records list 7 510(k) clearances for American Cyanamid Co., from to . As of , FDA records show no recalls naming K896946.

Clearance record

Decision date
Received
(145 days to decision)
Product code
FTM Mesh, Surgical
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
American Cyanamid Co. One Casper St., Danbury CT
Third party review
No

Clearances, product code FTM

Trailing 12 months
1 clearance under product code FTM in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260