Doro Radiolucent Headrest System and Horseshoe Headrests,And Non-Radiolucent J-Arm Retractor System (Aluminum Alloy)

Q: What is the product code of K032331?

The FDA product code is HBL – Holder, Head, Neurosurgical (Skull Clamp), a Class II (moderate risk) device regulated under 21 CFR 882.4460.

FDA 510(k) K032331 · Pro-Med Instruments GmbH

Substantially Equivalent

510(k) numberK032331

Submission

Device name: Doro Radiolucent Headrest System and Horseshoe Headrests,And Non-Radiolucent J-Arm Retractor System (Aluminum Alloy)
Applicant: Pro-Med Instruments GmbH
Alva, FL, US
Received: July 29, 2003
Decision date: November 20, 2003
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: HBL – Holder, Head, Neurosurgical (Skull Clamp)
Device class: Class II (moderate risk)
Regulation: 21 CFR 882.4460
Specialty: Neurology

Other 510(k)s with product code HBL

510(k)	Device	Applicant	Decision
K250423	mb-FIX Cranial Stabilization SystemsHBL · Traditional	Medical Bees GmbH	11/06/2025SE
K241883	DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00); DORO…HBL · Special	Pro Med Instruments GmbH	07/26/2024SE
K240319	DORO LUCENT Skull Clamp (1101.001); DORO LUCENT Skull Clamp Pediatric Set (1101.040)HBL · Traditional	Pro Med Instruments GmbH	04/24/2024SE
K203505	DORO QR3 Headrest System (Aluminum)HBL · Traditional	Pro Med Instruments GmbH	03/29/2021SE
K193438	DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile Disposable Skull…HBL · Traditional	Pro Med Instruments GmbH	06/02/2020SE
K191740	DORO LUCENT® iXI and iMRI Headrest SystemHBL · Traditional	Pro Med Instruments GmbH	02/21/2020SE
K191701	Arcus Head Fixation FrameHBL · Traditional	Mri Interventions, Inc.	11/15/2019SE
K191979	DORO QR3 XTom Headholder SystemHBL · Traditional	Pro Med Instruments GmbH	10/22/2019SE
K163322	TZ SKULL PIN AdultHBL · Traditional	Tz Medical, Inc.	02/23/2017SE
K142238	MAYFIELD Skull ClampHBL · Traditional	Integra LifeSciences Corporation	11/24/2014SE

More from Integra LifeSciences Corporation

510(k)	Device	Decision
K241883	DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00); DORO…HBL · Special	07/26/2024SE
K240319	DORO LUCENT Skull Clamp (1101.001); DORO LUCENT Skull Clamp Pediatric Set (1101.040)HBL · Traditional	04/24/2024SE
K203505	DORO QR3 Headrest System (Aluminum)HBL · Traditional	03/29/2021SE
K193438	DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile Disposable Skull…HBL · Traditional	06/02/2020SE
K191740	DORO LUCENT® iXI and iMRI Headrest SystemHBL · Traditional	02/21/2020SE
K191979	DORO QR3 XTom Headholder SystemHBL · Traditional	10/22/2019SE
K063494	Doro Radiolucent Headrest System ( Also Mri-Compatible) and ComponentsHBL · Traditional	05/21/2007SE
K070997	Doro Non-Stick Bipolar Forceps, Model 5001-XX to 5012-XX, Doro Bipolar Reusable Cables…GEI · Traditional	05/16/2007SE
K001808	Doro Headrest SystemHBL · Traditional	08/04/2000SE

Questions and answers

When was Doro Radiolucent Headrest System and Horseshoe Headrests,And Non-Radiolucent J-Arm Retractor System (Aluminum Alloy) cleared by the FDA?

Doro Radiolucent Headrest System and Horseshoe Headrests,And Non-Radiolucent J-Arm Retractor System (Aluminum Alloy) (K032331) received a 510(k) decision of Substantially Equivalent on November 20, 2003, 114 days after the submission was received.

What is the product code of K032331?

The FDA product code is HBL – Holder, Head, Neurosurgical (Skull Clamp), a Class II (moderate risk) device regulated under 21 CFR 882.4460.