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
K890285Substantially Equivalent

Prosthetic Cement Remover

Albert K. Chin, Portola Valley CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890285 is the FDA 510(k) clearance record for PROSTHETIC CEMENT REMOVER, a class II device, cleared for Albert K. Chin on under FDA product code LZV (System, Cement Removal Extraction). FDA records list one 510(k) clearance for Albert K. Chin. As of , FDA records show no recalls naming K890285.

Clearance record

Decision date
Received
(90 days to decision)
Product code
LZV System, Cement Removal Extraction
Regulation
21 CFR 888.4580
Device class
Class II
Review panel
Orthopedic
Applicant
Albert K. Chin 3274 Alpine Rd., Portola Valley CA
Third party review
No

Clearances, product code LZV

Trailing 12 months

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

FDA records show no clearances under product code LZV in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LZV, 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