Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K093464Substantially Equivalent

Rapidsorb Plus Screw System

Synthes (USA) Products LLC, West Chester PA / Traditional, Substantially Equivalent

K093464 is the FDA 510(k) clearance record for RAPIDSORB PLUS SCREW SYSTEM, a class II device, cleared for Synthes (Usa) on under FDA product code DZL (Screw, Fixation, Intraosseous). FDA records list 479 510(k) clearances for Synthes (USA) Products LLC, from to . As of , FDA records show no recalls naming K093464.

Clearance record

Decision date
Received
(80 days to decision)
Product code
DZL Screw, Fixation, Intraosseous
Regulation
21 CFR 872.4880
Device class
Class II
Review panel
Dental
Applicant
Synthes (Usa) 1230 Wilson Dr., West Chester PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DZL

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