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FDA 510(k)

PERNECZKY ANEURYSM CLIP

K-Number: K901312 · 1990-08-17

ApplicantVon Zeppelin GmbH
Decision Date1990-08-17
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PERNECZKY ANEURYSM CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Von Zeppelin GmbH. It received FDA 510(k) clearance on 1990-08-17 under 510(k) number K901312. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERNECZKY ANEURYSM CLIP?

PERNECZKY ANEURYSM CLIP is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Von Zeppelin GmbH. The 510(k) number is K901312.

When did PERNECZKY ANEURYSM CLIP receive FDA 510(k) clearance?

PERNECZKY ANEURYSM CLIP received FDA 510(k) clearance on 1990-08-17, under 510(k) number K901312.

Who is the listed applicant for PERNECZKY ANEURYSM CLIP?

The FDA 510(k) record lists Von Zeppelin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERNECZKY ANEURYSM CLIP?

The FDA product code for PERNECZKY ANEURYSM CLIP is HCH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Von Zeppelin GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K013091ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEMK954658PERNECZKY CLIP APPLIER/REMOVERK903151INTERVERTEBRAL DISC RONGEURK901313INSTRUMENTS FOR NEUROLOGICAL SURGERY

Related Devices (Code: HCH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K211183Sugita AVM MicroclipsMizuho America, Inc.K180757D-Clip; D-Clip ApplierPeter Lazic GmbHK091921CODMAN ANEURYSM CLIPS, CODMAN AVM MICRO CLIP SYSTEM, CODMAN SLIM-LINE GRAFT, REINFORCING, MINI ANEURYSM CLIPCodman & Shurtleff, Inc.K081640GIMMI ANEURYSM CLIPS AND APPLYING FORCEPSGimmi GmbHK081489L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERSPeter Lazic GmbHK060915KIRWAN L-ANEURYSM CLIPS AND APPLIER, KIRWAN YASARGIL-TYPE ANEURYSM CLIPS AND APPLIERSKirwan Surgical Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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