510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K973309Substantially Equivalent for Some Indications

Vilex Cannulated Bone Screw, Duval Cannulated Bone Screw

Vilex, Inc., Large PA / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K973309 is the FDA 510(k) clearance record for VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW, a class II device, cleared for Vilex, Inc. on under FDA product code HWC (Screw, Fixation, Bone). FDA records list one 510(k) clearance for Vilex, Inc. As of , FDA records show no recalls naming K973309.

Clearance record

Decision date
Received
(135 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Vilex, Inc. 811 Rt. 51, Industrial Complex, Large PA
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