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FDA 510(k)

ACE INTRAMEDULLARY ROD FOR SMALL BONES

K-Number: K850142 · 1985-02-07

ApplicantBuckman Co., Inc.
Decision Date1985-02-07
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE INTRAMEDULLARY ROD FOR SMALL BONES is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1985-02-07 under 510(k) number K850142. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE INTRAMEDULLARY ROD FOR SMALL BONES?

ACE INTRAMEDULLARY ROD FOR SMALL BONES is a medical device that received FDA 510(k) clearance on 1985-02-07. The listed applicant is Buckman Co., Inc.. The 510(k) number is K850142.

When did ACE INTRAMEDULLARY ROD FOR SMALL BONES receive FDA 510(k) clearance?

ACE INTRAMEDULLARY ROD FOR SMALL BONES received FDA 510(k) clearance on 1985-02-07, under 510(k) number K850142.

Who is the listed applicant for ACE INTRAMEDULLARY ROD FOR SMALL BONES?

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

What is the FDA product code for ACE INTRAMEDULLARY ROD FOR SMALL BONES?

The FDA product code for ACE INTRAMEDULLARY ROD FOR SMALL BONES is HSB.

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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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