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FDA 510(k)

KRONNER COLLES-FOREARM EXTERNAL FIXATION

K-Number: K871248 · 1987-06-03

ApplicantKronner Medical
Decision Date1987-06-03
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KRONNER COLLES-FOREARM 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 1987-06-03 under 510(k) number K871248. 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 COLLES-FOREARM EXTERNAL FIXATION?

KRONNER COLLES-FOREARM EXTERNAL FIXATION is a medical device that received FDA 510(k) clearance on 1987-06-03. The listed applicant is Kronner Medical. The 510(k) number is K871248.

When did KRONNER COLLES-FOREARM EXTERNAL FIXATION receive FDA 510(k) clearance?

KRONNER COLLES-FOREARM EXTERNAL FIXATION received FDA 510(k) clearance on 1987-06-03, under 510(k) number K871248.

Who is the listed applicant for KRONNER COLLES-FOREARM 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 COLLES-FOREARM EXTERNAL FIXATION?

The FDA product code for KRONNER COLLES-FOREARM 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 PINK871249KRONNER BI-PLANER TIBIA EXTERNAL FIXATIONK871247KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

View all 7 devices →

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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