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FDA 510(k)

KRONNER SPHERICAL CUTTERS

K-Number: K894228 · 1990-07-23

ApplicantKronner Medical
Decision Date1990-07-23
Product CodeHWT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KRONNER SPHERICAL CUTTERS is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Medical. It received FDA 510(k) clearance on 1990-07-23 under 510(k) number K894228. The device is classified under product code HWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KRONNER SPHERICAL CUTTERS?

KRONNER SPHERICAL CUTTERS is a medical device that received FDA 510(k) clearance on 1990-07-23. The listed applicant is Kronner Medical. The 510(k) number is K894228.

When did KRONNER SPHERICAL CUTTERS receive FDA 510(k) clearance?

KRONNER SPHERICAL CUTTERS received FDA 510(k) clearance on 1990-07-23, under 510(k) number K894228.

Who is the listed applicant for KRONNER SPHERICAL CUTTERS?

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 SPHERICAL CUTTERS?

The FDA product code for KRONNER SPHERICAL CUTTERS is HWT.

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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.

K895171BLOOD GAS SAFETY SYRINGEK895172KRONNER SACRAL PIN GUIDEK895173SKELETAL FIXATION PINK871248KRONNER COLLES-FOREARM EXTERNAL FIXATIONK871249KRONNER BI-PLANER TIBIA EXTERNAL FIXATIONK871247KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

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Related Devices (Code: HWT)

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.

K974406ORTHOPLANOrtho-Graphics, Inc.K960685ORTHODOC PREOPERATIVE PLANNER MODEL 500Integrated Surgical Systems, Inc.K870843SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIAWarsaw Orthopedic, Inc.K871323ARTHROSCOPIC MENISCAL SUTURE SYSTEMOrthopedic Systems, Inc.K8303603M OSTEOTOMY GUIDE3M CompanyK811205MOLDED POLYSULFONE TRIAL PROSTHESISShannon Group

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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