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FDA 510(k)

CHEMONUCLEOLYSIS TABLE #6100

K-Number: K832848 · 1983-10-04

ApplicantKirschner Medical Corp.
Decision Date1983-10-04
Product Code
DecisionSubstantially Equivalent

Device Summary

CHEMONUCLEOLYSIS TABLE #6100 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 1983-10-04 under 510(k) number K832848. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMONUCLEOLYSIS TABLE #6100?

CHEMONUCLEOLYSIS TABLE #6100 is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K832848.

When did CHEMONUCLEOLYSIS TABLE #6100 receive FDA 510(k) clearance?

CHEMONUCLEOLYSIS TABLE #6100 received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832848.

Who is the listed applicant for CHEMONUCLEOLYSIS TABLE #6100?

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

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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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