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FDA 510(k)

MERETE LOCKING BONE PLATE SYSTEM II

K-Number: K102688 · 2010-12-03

ApplicantMerete Medical GmbH
Decision Date2010-12-03
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MERETE LOCKING BONE PLATE SYSTEM II 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 2010-12-03 under 510(k) number K102688. 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 LOCKING BONE PLATE SYSTEM II?

MERETE LOCKING BONE PLATE SYSTEM II is a medical device that received FDA 510(k) clearance on 2010-12-03. The listed applicant is Merete Medical GmbH. The 510(k) number is K102688.

When did MERETE LOCKING BONE PLATE SYSTEM II receive FDA 510(k) clearance?

MERETE LOCKING BONE PLATE SYSTEM II received FDA 510(k) clearance on 2010-12-03, under 510(k) number K102688.

Who is the listed applicant for MERETE LOCKING BONE PLATE SYSTEM II?

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 LOCKING BONE PLATE SYSTEM II?

The FDA product code for MERETE LOCKING BONE PLATE SYSTEM II is KTT.

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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

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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.

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