510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903253Substantially Equivalent for Some Indications

Cancellous Screw

Onyx Medical LLC, Memphis TN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K903253 is the FDA 510(k) clearance record for CANCELLOUS SCREW, a class II device, cleared for Onyx Medical Corp. on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 48 510(k) clearances for Onyx Medical Corp., from to . As of , FDA records show no recalls naming K903253.

Clearance record

Decision date
Received
(16 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Onyx Medical Corp. 152 Collins St., Memphis TN
Third party review
No

Clearances, product code HWC

Trailing 12 months
21 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 20260