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FDA 510(k)

PLATE BLADE WITH CURSOR OF L'UNION

K-Number: K911021 · 1991-05-29

ApplicantSport Service, Inc.
Decision Date1991-05-29
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PLATE BLADE WITH CURSOR OF L'UNION is the device name listed in this FDA 510(k) record. The listed applicant is Sport Service, Inc.. It received FDA 510(k) clearance on 1991-05-29 under 510(k) number K911021. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLATE BLADE WITH CURSOR OF L'UNION?

PLATE BLADE WITH CURSOR OF L'UNION is a medical device that received FDA 510(k) clearance on 1991-05-29. The listed applicant is Sport Service, Inc.. The 510(k) number is K911021.

When did PLATE BLADE WITH CURSOR OF L'UNION receive FDA 510(k) clearance?

PLATE BLADE WITH CURSOR OF L'UNION received FDA 510(k) clearance on 1991-05-29, under 510(k) number K911021.

Who is the listed applicant for PLATE BLADE WITH CURSOR OF L'UNION?

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

What is the FDA product code for PLATE BLADE WITH CURSOR OF L'UNION?

The FDA product code for PLATE BLADE WITH CURSOR OF L'UNION is KTT.

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 Sport Service, 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.

K911020LIGAMENTOPLASTIC STAPLE OF L'UNIONK911031THE TRAMOND PINK911026STAPLE BLADE FOR TIBIAL OSTEO/STAPLE BLADE L'UNION

Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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