510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K941333Substantially Equivalent

Se5 Arthroscopy Sytem

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

K941333 is the FDA 510(k) clearance record for SE5 ARTHROSCOPY SYTEM, a class II device, cleared for Stryker Endoscopy on under FDA product code HRX (Arthroscope). FDA's definition for product code HRX reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 568 510(k) clearances for STRYKER CORP., from to . As of , FDA records show one recall naming K941333.

Clearance record

Decision date
Received
(237 days to decision)
Product code
HRX Arthroscope
Regulation
21 CFR 888.1100
Device class
Class II
Review panel
Orthopedic
Applicant
Stryker Endoscopy 210 Baypointe Pkwy., San Jose CA
510(k) summary
Summary
Third party review
No

Clearances, product code HRX

Trailing 12 months
10 clearances under product code HRX in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code HRX, trailing twelve months
MonthClearances
November 20252
December 20252
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20262
September 20260
October 20261