510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961971Substantially Equivalent

Q-5000

Stryker Corp., Santa Clara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K961971 is the FDA 510(k) clearance record for Q-5000, a class II device, cleared for Stryker Endoscopy on under FDA product code FSS (Light, Surgical, Floor Standing). FDA records list 568 510(k) clearances for STRYKER CORP., from to . As of , FDA records show no recalls naming K961971.

Clearance record

Decision date
Received
(39 days to decision)
Product code
FSS Light, Surgical, Floor Standing
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Stryker Endoscopy 2590 Walsh Ave., Santa Clara CA
510(k) summary
Summary
Third party review
No

Clearances, product code FSS

Trailing 12 months

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

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