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FDA 510(k)

LMT BONE ANCHOR

K-Number: K951472 · 1995-07-03

ApplicantLi Medical Technologies, Inc.
Decision Date1995-07-03
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LMT BONE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Li Medical Technologies, Inc.. It received FDA 510(k) clearance on 1995-07-03 under 510(k) number K951472. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LMT BONE ANCHOR?

LMT BONE ANCHOR is a medical device that received FDA 510(k) clearance on 1995-07-03. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K951472.

When did LMT BONE ANCHOR receive FDA 510(k) clearance?

LMT BONE ANCHOR received FDA 510(k) clearance on 1995-07-03, under 510(k) number K951472.

Who is the listed applicant for LMT BONE ANCHOR?

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

What is the FDA product code for LMT BONE ANCHOR?

The FDA product code for LMT BONE ANCHOR is HWC. This falls under the Cardiovascular category.

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Other records listing Li Medical Technologies, Inc. as applicant

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.

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Related Devices (Code: HWC)

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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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