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FDA 510(k)

CHEMONUCLEOLYSIS TABLE EXTENSION

K-Number: K831042 · 1983-05-16

Decision Date1983-05-16
Product CodeFSE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHEMONUCLEOLYSIS TABLE EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1983-05-16 under 510(k) number K831042. The device is classified under product code FSE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMONUCLEOLYSIS TABLE EXTENSION?

CHEMONUCLEOLYSIS TABLE EXTENSION is a medical device that received FDA 510(k) clearance on 1983-05-16. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K831042.

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

CHEMONUCLEOLYSIS TABLE EXTENSION received FDA 510(k) clearance on 1983-05-16, under 510(k) number K831042.

Who is the listed applicant for CHEMONUCLEOLYSIS TABLE EXTENSION?

The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEMONUCLEOLYSIS TABLE EXTENSION?

The FDA product code for CHEMONUCLEOLYSIS TABLE EXTENSION is FSE.

Related Clinical Trials

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.

Other records listing Orthopedic Systems, Inc. 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.

View all 95 devices →

Related Devices (Code: FSE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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