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FDA 510(k)

OSSTAPLE

K-Number: K023203 · 2002-10-17

ApplicantBiomedical Ent., Inc.
Decision Date2002-10-17
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSSTAPLE 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 2002-10-17 under 510(k) number K023203. 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 OSSTAPLE?

OSSTAPLE is a medical device that received FDA 510(k) clearance on 2002-10-17. The listed applicant is Biomedical Ent., Inc.. The 510(k) number is K023203.

When did OSSTAPLE receive FDA 510(k) clearance?

OSSTAPLE received FDA 510(k) clearance on 2002-10-17, under 510(k) number K023203.

Who is the listed applicant for OSSTAPLE?

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 OSSTAPLE?

The FDA product code for OSSTAPLE 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 CHILLK091951HAMMERLOCKK001354MEMOGRAPH; OSSTAPLE - ORTHOPEDIC USES FOR SMALL BONE AND FRAGMENT FIXATION FOR THE MEMOGRAPH STAPLE SYSTEMK001353MEMOGRAPH; OSSTAPLE - NEUROSURGICAL USES FOR CRANIOFACIAL FRACTURES AND CRANIOPLASTY FOR THE MEMOGRAPH STAPLE SYSTEMK001219MEMOGRAPH; OSSTAPLE - ORAL AND MAXILLIOFACIAL PROCEDURES FOR THE MEMOGRAPH STAPLE SYSTEM

View all 11 devices →

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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