510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K220319Substantially Equivalent

Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System

Stryker Corp., Mahwah NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220319 is the FDA 510(k) clearance record for Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System, a class II device, cleared for Stryker GmbH on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 568 510(k) clearances for Stryker GmbH, from to . As of , FDA records show no recalls naming K220319.

Clearance record

Decision date
Received
(127 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Stryker GmbH 325 Corporate Dr., Mahwah NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HWC

Trailing 12 months
22 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20261