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FDA 510(k)

IMPLANTOFIX

K-Number: K851293 · 1986-01-09

ApplicantBurron Medical Products, Inc.
Decision Date1986-01-09
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMPLANTOFIX is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1986-01-09 under 510(k) number K851293. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTOFIX?

IMPLANTOFIX is a medical device that received FDA 510(k) clearance on 1986-01-09. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K851293.

When did IMPLANTOFIX receive FDA 510(k) clearance?

IMPLANTOFIX received FDA 510(k) clearance on 1986-01-09, under 510(k) number K851293.

Who is the listed applicant for IMPLANTOFIX?

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

What is the FDA product code for IMPLANTOFIX?

The FDA product code for IMPLANTOFIX is LJT.

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Related Devices (Code: LJT)

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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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