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FDA 510(k)

SEGMENTAL SPINAL INSTRUMENTATION SYSTEM

K-Number: K864337 · 1986-12-16

ApplicantKirschner Medical Corp.
Decision Date1986-12-16
Product Code
DecisionSubstantially Equivalent

Device Summary

SEGMENTAL SPINAL INSTRUMENTATION SYSTEM 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 1986-12-16 under 510(k) number K864337. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEGMENTAL SPINAL INSTRUMENTATION SYSTEM?

SEGMENTAL SPINAL INSTRUMENTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K864337.

When did SEGMENTAL SPINAL INSTRUMENTATION SYSTEM receive FDA 510(k) clearance?

SEGMENTAL SPINAL INSTRUMENTATION SYSTEM received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864337.

Who is the listed applicant for SEGMENTAL SPINAL INSTRUMENTATION SYSTEM?

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

Related Clinical Trials

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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

View all 76 devices →

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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