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FDA 510(k)

STRYKER MICRODEBRIDER SYSTEM

K-Number: K940710 · 1994-05-16

ApplicantStryker Corp.
Decision Date1994-05-16
Product CodeERL
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

STRYKER MICRODEBRIDER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K940710. The device is classified under product code ERL. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER MICRODEBRIDER SYSTEM?

STRYKER MICRODEBRIDER SYSTEM is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is Stryker Corp.. The 510(k) number is K940710.

When did STRYKER MICRODEBRIDER SYSTEM receive FDA 510(k) clearance?

STRYKER MICRODEBRIDER SYSTEM received FDA 510(k) clearance on 1994-05-16, under 510(k) number K940710.

Who is the listed applicant for STRYKER MICRODEBRIDER SYSTEM?

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

What is the FDA product code for STRYKER MICRODEBRIDER SYSTEM?

The FDA product code for STRYKER MICRODEBRIDER SYSTEM is ERL.

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Other records listing Stryker Corp. 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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Related Devices (Code: ERL)

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.

K243280Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories)W&H Dentalwerk Buermoos GmbHK233958hekaDrillZethon, Ltd.K221184ORiGO SystemBien-Air Surgery SAK213221AMADEO, M-UK1015 (incl. attachments and accessories)W&H Dentalwerk Buermoss GmbHK212650Celeris, Disposable Sinus DebriderGyrus Acmi, Inc.K211490Pi Drive 2 Motor / Model Number 5407-150-000, Pi Drive 2 Plus Motor / Model Number 5407-350-000Stryker Corporation

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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