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FDA 510(k)

LM ANCHOR OR OTHER PROPRIETARY NAME

K-Number: K960825 · 1996-04-30

ApplicantLi Medical Technologies, Inc.
Decision Date1996-04-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LM ANCHOR OR OTHER PROPRIETARY NAME 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 1996-04-30 under 510(k) number K960825. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LM ANCHOR OR OTHER PROPRIETARY NAME?

LM ANCHOR OR OTHER PROPRIETARY NAME is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K960825.

When did LM ANCHOR OR OTHER PROPRIETARY NAME receive FDA 510(k) clearance?

LM ANCHOR OR OTHER PROPRIETARY NAME received FDA 510(k) clearance on 1996-04-30, under 510(k) number K960825.

Who is the listed applicant for LM ANCHOR OR OTHER PROPRIETARY NAME?

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 LM ANCHOR OR OTHER PROPRIETARY NAME?

The FDA product code for LM ANCHOR OR OTHER PROPRIETARY NAME is MBI.

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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.

K002413ULTRASORB SUTURE ANCHORK993373ROTORBLADE SUTURE ANCHORK992938ROTORBLADE SUTURE ANCHORK983435ROTORBLADEK981755LM ANCHORK981764LM ANCHOR

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Related Devices (Code: MBI)

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.

K261869Integrity Retractable Implant Inserter (6000127)Anika Therapeutics, Inc.K262809ArthroTAK Tendon Anchor KitArthroTAK, LLCK253065Aevumed SUPERCYNCH™ Button SystemAevumed, Inc.K262677Iconix Knotless TRiverpoint MedicalK262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker Endoscopy

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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