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FDA 510(k)

KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

K-Number: K871247 · 1987-05-22

ApplicantKronner Medical
Decision Date1987-05-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KRONNER UNIVERSAL FRAME EXTERNAL FIXATION is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Medical. It received FDA 510(k) clearance on 1987-05-22 under 510(k) number K871247. 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 KRONNER UNIVERSAL FRAME EXTERNAL FIXATION?

KRONNER UNIVERSAL FRAME EXTERNAL FIXATION is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Kronner Medical. The 510(k) number is K871247.

When did KRONNER UNIVERSAL FRAME EXTERNAL FIXATION receive FDA 510(k) clearance?

KRONNER UNIVERSAL FRAME EXTERNAL FIXATION received FDA 510(k) clearance on 1987-05-22, under 510(k) number K871247.

Who is the listed applicant for KRONNER UNIVERSAL FRAME EXTERNAL FIXATION?

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

What is the FDA product code for KRONNER UNIVERSAL FRAME EXTERNAL FIXATION?

The FDA product code for KRONNER UNIVERSAL FRAME EXTERNAL FIXATION is KTT.

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Other records listing Kronner Medical 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.

K894228KRONNER SPHERICAL CUTTERSK895171BLOOD GAS SAFETY SYRINGEK895172KRONNER SACRAL PIN GUIDEK895173SKELETAL FIXATION PINK871248KRONNER COLLES-FOREARM EXTERNAL FIXATIONK871249KRONNER BI-PLANER TIBIA EXTERNAL FIXATION

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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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