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FDA 510(k)

PSI TITANIUM ANEURYSM CLIP

K-Number: K991959 · 2000-01-06

ApplicantV. Mueller Neuro/Spine
Decision Date2000-01-06
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PSI TITANIUM ANEURYSM CLIP is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller Neuro/Spine. It received FDA 510(k) clearance on 2000-01-06 under 510(k) number K991959. 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 PSI TITANIUM ANEURYSM CLIP?

PSI TITANIUM ANEURYSM CLIP is a medical device that received FDA 510(k) clearance on 2000-01-06. The listed applicant is V. Mueller Neuro/Spine. The 510(k) number is K991959.

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

PSI TITANIUM ANEURYSM CLIP received FDA 510(k) clearance on 2000-01-06, under 510(k) number K991959.

Who is the listed applicant for PSI TITANIUM ANEURYSM CLIP?

The FDA 510(k) record lists V. Mueller Neuro/Spine as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PSI TITANIUM ANEURYSM CLIP?

The FDA product code for PSI TITANIUM ANEURYSM CLIP is HCH.

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Other records listing V. Mueller Neuro/Spine 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.

K002276PSI SKULL CLAMPK993019PACIFIC SURGICAL PATTIESK991002PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIPK972750TAKA ANEURYSM CLIPK964402VERSATRAC (TM) LUMBAR RETRACTOR SYSTEMK942601PSI FLEXIBLE ARM

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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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