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FDA 510(k)

MEMOGRAPH STAPLE, WARM SYSTEM

K-Number: K993714 · 2000-02-25

ApplicantBiomedical Ent., Inc.
Decision Date2000-02-25
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMOGRAPH STAPLE, WARM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Ent., Inc.. It received FDA 510(k) clearance on 2000-02-25 under 510(k) number K993714. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMOGRAPH STAPLE, WARM SYSTEM?

MEMOGRAPH STAPLE, WARM SYSTEM is a medical device that received FDA 510(k) clearance on 2000-02-25. The listed applicant is Biomedical Ent., Inc.. The 510(k) number is K993714.

When did MEMOGRAPH STAPLE, WARM SYSTEM receive FDA 510(k) clearance?

MEMOGRAPH STAPLE, WARM SYSTEM received FDA 510(k) clearance on 2000-02-25, under 510(k) number K993714.

Who is the listed applicant for MEMOGRAPH STAPLE, WARM SYSTEM?

The FDA 510(k) record lists Biomedical Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEMOGRAPH STAPLE, WARM SYSTEM?

The FDA product code for MEMOGRAPH STAPLE, WARM SYSTEM is JDR.

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Other records listing Biomedical Ent., Inc. 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.

K131640SMOOTH OR THREADED METALLIC BONE FASTENERK102107OSSTAPLE CHILLK091951HAMMERLOCKK023203OSSTAPLEK001353MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEMK001354MEMOGRAPH; OSSTAPLE - ORTHOPEDIC USES FOR SMALL BONE AND FRAGMENT FIXATION FOR THE MEMOGRAPH STAPLE SYSTEM

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Related Devices (Code: JDR)

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.

K262451Arthrex DynaNite StaplesArthrex, Inc.K261121Megalodon Dynamic Compression SystemParagon 28, Inc.K250712Linkt Compression Staple SystemTrax SurgicalK243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LPK243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.K243658TMC Compression Implant SystemTreace Medical Concepts

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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