510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955599Substantially Equivalent

Stryker Femoral Canal Sponge & Acetabulum Sponge

Stryker Corp., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955599 is the FDA 510(k) clearance record for STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE, a class I device, cleared for Stryker Corp. on under FDA product code GDY (Gauze/Sponge, Internal, X-Ray Detectable). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show 5 recalls naming K955599.

Clearance record

Decision date
Received
(76 days to decision)
Product code
GDY Gauze/Sponge, Internal, X-Ray Detectable
Regulation
21 CFR 878.4450
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Stryker Corp. 2725 Fairfield Rd., Kalamazoo MI
510(k) summary
Statement
Third party review
No

Clearances, product code GDY

Trailing 12 months

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

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