Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LM BONE ANCHOR (ORTHOPEDICS)

K-Number: K963812 · 1996-11-12

ApplicantLi Medical Technologies, Inc.
Decision Date1996-11-12
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LM BONE ANCHOR (ORTHOPEDICS) 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 1996-11-12 under 510(k) number K963812. 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 BONE ANCHOR (ORTHOPEDICS)?

LM BONE ANCHOR (ORTHOPEDICS) is a medical device that received FDA 510(k) clearance on 1996-11-12. The listed applicant is Li Medical Technologies, Inc.. The 510(k) number is K963812.

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

LM BONE ANCHOR (ORTHOPEDICS) received FDA 510(k) clearance on 1996-11-12, under 510(k) number K963812.

Who is the listed applicant for LM BONE ANCHOR (ORTHOPEDICS)?

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 BONE ANCHOR (ORTHOPEDICS)?

The FDA product code for LM BONE ANCHOR (ORTHOPEDICS) is MBI.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 17 devices →

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.

↑