510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K121573Substantially Equivalent

Integra Camino Icp Monitor

Intrgra Lifesciences Corporation, Planisboro NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121573 is the FDA 510(k) clearance record for INTEGRA CAMINO ICP MONITOR, a class II device, cleared for Intrgra Lifesciences Corporation on under FDA product code GWM (Device, Monitoring, Intracranial Pressure). FDA records list one 510(k) clearance for Intrgra Lifesciences Corporation. As of , FDA records show 3 recalls naming K121573.

Clearance record

Decision date
Received
(104 days to decision)
Product code
GWM Device, Monitoring, Intracranial Pressure
Regulation
21 CFR 882.1620
Device class
Class II
Review panel
Neurology
Applicant
Intrgra Lifesciences Corporation 311 Enterprise Dr., Planisboro NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWM

Trailing 12 months
1 clearance under product code GWM in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260