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
K180150Substantially Equivalent

PL8 Wrist Reconstruction Plate

Citieffe Inc., Calderara Di Reno, IT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K180150 is the FDA 510(k) clearance record for PL8 Wrist Reconstruction Plate, a class II device, cleared for Citieffe S.R.L. on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 11 510(k) clearances for Citieffe S.R.L., from to . As of , FDA records show no recalls naming K180150.

Clearance record

Decision date
Received
(195 days to decision)
Product code
HRS Plate, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Citieffe S.R.L. Via Armaroli 21, Calderara Di Reno, IT
510(k) summary
Statement
Third party review
No

Clearances, product code HRS

Trailing 12 months
57 clearances under product code HRS in the twelve months to October 2026, March 2026 the highest month at 13.
Show the numbers
Monthly 510(k) clearances under FDA product code HRS, trailing twelve months
MonthClearances
November 20255
December 20255
January 20264
February 20265
March 202613
April 20266
May 20262
June 20265
July 20265
August 20263
September 20264
October 20260