510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850886Substantially Equivalent

Compression Hip Screw System

Pfizer Inc, Ny NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850886 is the FDA 510(k) clearance record for COMPRESSION HIP SCREW SYSTEM, a class I device, cleared for Pfizer, Inc. on under FDA product code KIT (Media And Components, Synthetic Cell And Tissue Culture). FDA records list 30 510(k) clearances for Pfizer, Inc., from to . As of , FDA records show one recall naming K850886.

Clearance record

Decision date
Received
(46 days to decision)
Product code
KIT Media And Components, Synthetic Cell And Tissue Culture
Regulation
21 CFR 864.2220
Device class
Class I
Review panel
Hematology
Applicant
Pfizer, Inc. 235 E. 42nd St., Ny NY
Third party review
No

Clearances, product code KIT

Trailing 12 months

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

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