510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072207Substantially Equivalent

Duragen Xs Dural Regeneration Matrix

Integra LifeSciences Corporation, Plainsboro NJ / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072207 is the FDA 510(k) clearance record for DURAGEN XS DURAL REGENERATION MATRIX, a class II device, cleared for Integra Lifesciences Corp. on under FDA product code GXQ (Dura Substitute). FDA records list 94 510(k) clearances for Integra Lifesciences Corp., from to . As of , FDA records show 6 recalls naming K072207.

Clearance record

Decision date
Received
(15 days to decision)
Product code
GXQ Dura Substitute
Regulation
21 CFR 882.5910
Device class
Class II
Review panel
Neurology
Applicant
Integra Lifesciences Corp. 311c Enterprise Dr., Plainsboro NJ
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