Chemonucleolysis Table Extension

FDA 510(k) K831042 · Orthopedic Systems, Inc.

Substantially Equivalent

510(k) numberK831042

Submission

Device name
Chemonucleolysis Table Extension
Applicant
Orthopedic Systems, Inc.
Mchenry, IL, US
Received
March 31, 1983
Decision date
May 16, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FSE – Table, Operating-Room, Manual
Device class
Class I (low risk)
Regulation
21 CFR 878.4950
Specialty
General, Plastic Surgery

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Questions and answers

When was Chemonucleolysis Table Extension cleared by the FDA?

Chemonucleolysis Table Extension (K831042) received a 510(k) decision of Substantially Equivalent on May 16, 1983, 46 days after the submission was received.

What is the product code of K831042?

The FDA product code is FSE – Table, Operating-Room, Manual, a Class I (low risk) device regulated under 21 CFR 878.4950.