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FDA 510(k)

EASYLOCK OSTEOSYSTEM

K-Number: K111266 · 2011-10-06

ApplicantTriMed, Inc.
Decision Date2011-10-06
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EASYLOCK OSTEOSYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is TriMed, Inc.. It received FDA 510(k) clearance on 2011-10-06 under 510(k) number K111266. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYLOCK OSTEOSYSTEM?

EASYLOCK OSTEOSYSTEM is a medical device that received FDA 510(k) clearance on 2011-10-06. The listed applicant is TriMed, Inc.. The 510(k) number is K111266.

When did EASYLOCK OSTEOSYSTEM receive FDA 510(k) clearance?

EASYLOCK OSTEOSYSTEM received FDA 510(k) clearance on 2011-10-06, under 510(k) number K111266.

Who is the listed applicant for EASYLOCK OSTEOSYSTEM?

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

What is the FDA product code for EASYLOCK OSTEOSYSTEM?

The FDA product code for EASYLOCK OSTEOSYSTEM is HRS.

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Other records listing TriMed, Inc. as applicant

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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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