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FDA 510(k)

RUBIN BONE PLANER W/REPLACEABLE BLADE

K-Number: K884473 · 1988-12-09

ApplicantNeo Contemporary Co.
Decision Date1988-12-09
Product CodeGAC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RUBIN BONE PLANER W/REPLACEABLE BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Neo Contemporary Co.. It received FDA 510(k) clearance on 1988-12-09 under 510(k) number K884473. The device is classified under product code GAC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBIN BONE PLANER W/REPLACEABLE BLADE?

RUBIN BONE PLANER W/REPLACEABLE BLADE is a medical device that received FDA 510(k) clearance on 1988-12-09. The listed applicant is Neo Contemporary Co.. The 510(k) number is K884473.

When did RUBIN BONE PLANER W/REPLACEABLE BLADE receive FDA 510(k) clearance?

RUBIN BONE PLANER W/REPLACEABLE BLADE received FDA 510(k) clearance on 1988-12-09, under 510(k) number K884473.

Who is the listed applicant for RUBIN BONE PLANER W/REPLACEABLE BLADE?

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

What is the FDA product code for RUBIN BONE PLANER W/REPLACEABLE BLADE?

The FDA product code for RUBIN BONE PLANER W/REPLACEABLE BLADE is GAC.

Related Clinical Trials

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Related Devices (Code: GAC)

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.

K853601MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASPBowen & Company, Inc.

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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