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FDA 510(k)

BONALIVE GRANULES AND BONALIVE PLATES

K-Number: K071937 · 2007-10-19

ApplicantVivoxid , Ltd.
Decision Date2007-10-19
Product CodeKKY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BONALIVE GRANULES AND BONALIVE PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Vivoxid , Ltd.. It received FDA 510(k) clearance on 2007-10-19 under 510(k) number K071937. The device is classified under product code KKY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONALIVE GRANULES AND BONALIVE PLATES?

BONALIVE GRANULES AND BONALIVE PLATES is a medical device that received FDA 510(k) clearance on 2007-10-19. The listed applicant is Vivoxid , Ltd.. The 510(k) number is K071937.

When did BONALIVE GRANULES AND BONALIVE PLATES receive FDA 510(k) clearance?

BONALIVE GRANULES AND BONALIVE PLATES received FDA 510(k) clearance on 2007-10-19, under 510(k) number K071937.

Who is the listed applicant for BONALIVE GRANULES AND BONALIVE PLATES?

The FDA 510(k) record lists Vivoxid , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONALIVE GRANULES AND BONALIVE PLATES?

The FDA product code for BONALIVE GRANULES AND BONALIVE PLATES is KKY.

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 Vivoxid , Ltd. 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.

K071199BONALIVE GRANULESK070055BONALIVE GRANULES AND BONALIVE PLATES

Related Devices (Code: KKY)

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.

K211514Longeviti PorousFit implantLongeviti Neuro Solutions, LLCK161052OsteoFab Patient Specific Facial DeviceOxford Performance Materials, Inc.K160988Biopor, AOC Porous Polyethylene, CereporCeremed , Inc.K123908OMNIPORE SURGICAL IMPLANTS AND ACCESSORIESMatrix Surgical USAK111323SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTSSynthes, Inc.K103010STRYKER PATIENT SPECIFIC POLYMER IMPLANTHowmedica Osteonics Corp., Dba Stryker Orthopaedics

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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