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)

MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE

K-Number: K063487 · 2007-01-22

ApplicantMerete Medical GmbH
Decision Date2007-01-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Merete Medical GmbH. It received FDA 510(k) clearance on 2007-01-22 under 510(k) number K063487. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE?

MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE is a medical device that received FDA 510(k) clearance on 2007-01-22. The listed applicant is Merete Medical GmbH. The 510(k) number is K063487.

When did MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE receive FDA 510(k) clearance?

MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE received FDA 510(k) clearance on 2007-01-22, under 510(k) number K063487.

Who is the listed applicant for MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE?

The FDA 510(k) record lists Merete Medical GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE?

The FDA product code for MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE is KTT.

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 Merete Medical GmbH 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.

K160548MC-Subtalar(TM) IIK152187MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws and TwistCut Snap-Off ScrewsK132226METAFIX BLP PLATE, SIZE 31, LEFT, METAFIX BLP PLATE, SIZE 31,RIGHTK123619INTRABLOCK BIOBALL HIP SYSTEM (IBS)K130400MERETEC CS, CORTICAL SCREWSK120787MERETE LOCKING BONE PLATE SYSTEM III

View all 20 devices →

Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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.

↑