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FDA 510(k)

MBS HARD TISSUE REPLACEMENT SYSTEM

K-Number: K832509 · 1983-11-29

Decision Date1983-11-29
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MBS HARD TISSUE REPLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Biological Sciences, Inc.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K832509. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MBS HARD TISSUE REPLACEMENT SYSTEM?

MBS HARD TISSUE REPLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Medical Biological Sciences, Inc.. The 510(k) number is K832509.

When did MBS HARD TISSUE REPLACEMENT SYSTEM receive FDA 510(k) clearance?

MBS HARD TISSUE REPLACEMENT SYSTEM received FDA 510(k) clearance on 1983-11-29, under 510(k) number K832509.

Who is the listed applicant for MBS HARD TISSUE REPLACEMENT SYSTEM?

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

What is the FDA product code for MBS HARD TISSUE REPLACEMENT SYSTEM?

The FDA product code for MBS HARD TISSUE REPLACEMENT SYSTEM is LYC.

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.

Related Devices (Code: LYC)

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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