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FDA 510(k)

KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE

K-Number: K901234 · 1990-10-04

ApplicantKirschner Medical Corp.
Decision Date1990-10-04
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K901234. 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 KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE?

KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K901234.

When did KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE receive FDA 510(k) clearance?

KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE received FDA 510(k) clearance on 1990-10-04, under 510(k) number K901234.

Who is the listed applicant for KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE?

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

What is the FDA product code for KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE?

The FDA product code for KIRSCHNER BLADE PLATE SYSTEM OR R.A.B. BLADE PLATE is KTT.

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Other records listing Kirschner Medical Corp. 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.

K940537KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEMK936274KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEMK942891SUMMIT TOTAL HIP SYSTEMK941486INTEGRITY TOTAL HIP SYSTEM, NON-POROUSK933843LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATEDK935951KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM

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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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