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FDA 510(k)

CHEMONUCLEOLYSIS TABLE

K-Number: K833509 · 1983-11-28

ApplicantStryker Corp.
Decision Date1983-11-28
Product CodeFWY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHEMONUCLEOLYSIS TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833509. The device is classified under product code FWY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMONUCLEOLYSIS TABLE?

CHEMONUCLEOLYSIS TABLE is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Stryker Corp.. The 510(k) number is K833509.

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

CHEMONUCLEOLYSIS TABLE received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833509.

Who is the listed applicant for CHEMONUCLEOLYSIS TABLE?

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

What is the FDA product code for CHEMONUCLEOLYSIS TABLE?

The FDA product code for CHEMONUCLEOLYSIS TABLE is FWY.

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Other records listing Stryker Corp. as applicant

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K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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Related Devices (Code: FWY)

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.

K883457ASST-3000 SPINAL SURGERY TABLEOrthopedic Systems, Inc.K873478SKYTRON MODEL 130 SURGICAL TABLESkytron, Div. the Kmw Group, Inc.K800118CHICK SURGICAL TABLEWarner-Lambert Co.

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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