510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K152481Substantially Equivalent

DURAFORM Dural Graft Implant

Cerenovus, Inc., Raynham MA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152481 is the FDA 510(k) clearance record for DURAFORM Dural Graft Implant, a class II device, cleared for Codman & Shurtleff, Inc. on under FDA product code GXQ (Dura Substitute). FDA records list 163 510(k) clearances for Cerenovus, Inc., from to . As of , FDA records show one recall naming K152481.

Clearance record

Decision date
Received
(60 days to decision)
Product code
GXQ Dura Substitute
Regulation
21 CFR 882.5910
Device class
Class II
Review panel
Neurology
Applicant
Codman & Shurtleff, Inc. 325 Paramount Dr., Raynham MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXQ

Trailing 12 months
1 clearance under product code GXQ in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GXQ, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260