510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920526Substantially Equivalent

Stryker Dynamic Mattress System (Dms) Model #2500

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

K920526 is the FDA 510(k) clearance record for STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500, a class I device, cleared for Stryker Medical on under FDA product code IOG (Treadmill, Mechanical). FDA records list 14 510(k) clearances for Stryker Medical, from to . As of , FDA records show no recalls naming K920526.

Clearance record

Decision date
Received
(230 days to decision)
Product code
IOG Treadmill, Mechanical
Regulation
21 CFR 890.5370
Device class
Class I
Review panel
Physical Medicine
Applicant
Stryker Medical 6300 S. Sprinkle Rd., Kalamazoo MI
510(k) summary
Statement
Third party review
No

Clearances, product code IOG

Trailing 12 months

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

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