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FDA 510(k)

ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM

K-Number: K013091 · 2002-01-25

ApplicantVon Zeppelin GmbH
Decision Date2002-01-25
Product CodeHBB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM 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 2002-01-25 under 510(k) number K013091. The device is classified under product code HBB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM?

ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-01-25. The listed applicant is Von Zeppelin GmbH. The 510(k) number is K013091.

When did ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM receive FDA 510(k) clearance?

ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM received FDA 510(k) clearance on 2002-01-25, under 510(k) number K013091.

Who is the listed applicant for ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM?

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 ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM?

The FDA product code for ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM is HBB.

Related Clinical Trials

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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.

K954658PERNECZKY CLIP APPLIER/REMOVERK903151INTERVERTEBRAL DISC RONGEURK901312PERNECZKY ANEURYSM CLIPK901313INSTRUMENTS FOR NEUROLOGICAL SURGERY

Related Devices (Code: HBB)

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.

K253772Velocity Alpha MR High Speed Surgical Drill SystemAdeor Medical AGK172907ELAN 4 Air Motor SystemAesculap, Inc.K163182Medtronic Legend Pneumatic; MR7 Pneumatic; Triton Pneumatic Drill System incorporating various Pneumatic Handpieces; Attachments; Surgical Dissecting Tools; and System AccessoriesMedtronic Powered Surgical SolutionsK101168LEGEND POWER ADAPTER MODEL: 6475000Medtronic Sofamor DanekK093361SYNTHES AIR PEN DRIVE (APD) SYSTEMSynthes (Usa)K090112MIDAS REX MR7 PNEUMATIC HIGH SPEED SYSTEM, MODELS PM700, PM710, PC700, PC710, PC720, PA700Medtronic Powered Surgical Solutions

Official Source

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

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