FDA 510(k)

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM

K-Number: K993990 · 2000-02-22

Decision Date2000-02-22

Product CodeGXN

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2000-02-22 under 510(k) number K993990. The device is classified under product code GXN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM?

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM is a medical device that received FDA 510(k) clearance on 2000-02-22. The listed applicant is Stryker Instruments. The 510(k) number is K993990.

When did LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM receive FDA 510(k) clearance?

LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM received FDA 510(k) clearance on 2000-02-22, under 510(k) number K993990.

Who is the listed applicant for LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM?

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

What is the FDA product code for LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM?

The FDA product code for LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM is GXN.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stryker Instruments as applicant

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)K261544Hydro Irrigation System K253679Hydro Irrigation System K252282SurgiCount+ System K251971RPS Primary TKA Software; RPS Console; RPS Saw One; RPS Cable; RPS Saw Oscillating Tip Cartridge; RPS Console Cart Attachment; Ball Tip Pointer K250483PhotonBlade 3; PhotonBlade 3 Smoke Evacuation

View all 75 devices →

Related Devices (Code: GXN)

K260709ClearFit Ti Ring 14mm (171750);ClearFit Ti Ring 14mm with Slot (171751);ClearFit Ti Ring 20mm (171752);ClearFit Ti Ring 20mm with Slot (171753);ClearFit Ti Ring 30mm (171754)Longeviti Neuro Solutions K2531163D MAC Titanium Cranial Plate (TCP) SystemThe Surgeon General, Department of the Army (TSG-DA)K252251EASYMADE-TICG Bio Co., Ltd.K252958METICULY Patient-specific titanium mesh implantMeticuly Co., Ltd.K243715Synthes Patient Specific ImplantsSynthes GmbH K252573KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILEKLS-Martin L.P.

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.