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FDA 510(k)

FRIEDL GLIDING NAIL SYSTEM

K-Number: K974409 · 1998-02-19

ApplicantPlus Orthopedics
Decision Date1998-02-19
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FRIEDL GLIDING NAIL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Plus Orthopedics. It received FDA 510(k) clearance on 1998-02-19 under 510(k) number K974409. 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 FRIEDL GLIDING NAIL SYSTEM?

FRIEDL GLIDING NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 1998-02-19. The listed applicant is Plus Orthopedics. The 510(k) number is K974409.

When did FRIEDL GLIDING NAIL SYSTEM receive FDA 510(k) clearance?

FRIEDL GLIDING NAIL SYSTEM received FDA 510(k) clearance on 1998-02-19, under 510(k) number K974409.

Who is the listed applicant for FRIEDL GLIDING NAIL SYSTEM?

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

What is the FDA product code for FRIEDL GLIDING NAIL SYSTEM?

The FDA product code for FRIEDL GLIDING NAIL SYSTEM is KTT.

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Other records listing Plus Orthopedics 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.

K032126PROMOS SHOULDERK033763MODIFICATION TO SLIM GLIDING NAIL SYSTEMK032709MODULAR PLUS HIP STEMK032548IP-XS COMPRESSION NAIL SYSTEMK032215VKS/TC-PLUS REVISION KNEEK032052UC-PLUS SOLUTION UNICONDYLAR KNEE

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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

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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