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FDA 510(k)

CROSS PIN

K-Number: K961920 · 1996-09-17

ApplicantMedicinelodge, Inc.
Decision Date1996-09-17
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CROSS PIN is the device name listed in this FDA 510(k) record. The listed applicant is Medicinelodge, Inc.. It received FDA 510(k) clearance on 1996-09-17 under 510(k) number K961920. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROSS PIN?

CROSS PIN is a medical device that received FDA 510(k) clearance on 1996-09-17. The listed applicant is Medicinelodge, Inc.. The 510(k) number is K961920.

When did CROSS PIN receive FDA 510(k) clearance?

CROSS PIN received FDA 510(k) clearance on 1996-09-17, under 510(k) number K961920.

Who is the listed applicant for CROSS PIN?

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

What is the FDA product code for CROSS PIN?

The FDA product code for CROSS PIN is JDW.

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.

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Other records listing Medicinelodge, 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.

K072525ZIPKNOT, MODEL 1017-3000K051488MEDICINELODGE ZIPKNOTK962705MLI MODULAR STAPLEK961905MEDICINELODGE, INC. SET SCREWK962194MLI SOFT TISSUE SCREW & WASHER SYSTEMK961025EXPANDED BODY SUTURE

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Related Devices (Code: JDW)

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.

K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmBiodynamik, Inc.K250316Meduloc Intramedullary Fracture Fixation (IFF) SystemMeduloc, LLCK241357XT3 SystemBiodynamik, Inc.K223112MAVERICK Mini External Fixation SystemSmith & Nephew, Inc.K213874MAVERICK External Fixation SystemSmith & Nephew, Inc.K211508Steinmann Pins and Kirschner WiresStryker GmbH

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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