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FDA 510(k)

CERAMENT BONE VOID FILLER, MODEL A0210

K-Number: K073316 · 2008-06-20

ApplicantBonesupport AB
Decision Date2008-06-20
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERAMENT BONE VOID FILLER, MODEL A0210 is the device name listed in this FDA 510(k) record. The listed applicant is Bonesupport AB. It received FDA 510(k) clearance on 2008-06-20 under 510(k) number K073316. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERAMENT BONE VOID FILLER, MODEL A0210?

CERAMENT BONE VOID FILLER, MODEL A0210 is a medical device that received FDA 510(k) clearance on 2008-06-20. The listed applicant is Bonesupport AB. The 510(k) number is K073316.

When did CERAMENT BONE VOID FILLER, MODEL A0210 receive FDA 510(k) clearance?

CERAMENT BONE VOID FILLER, MODEL A0210 received FDA 510(k) clearance on 2008-06-20, under 510(k) number K073316.

Who is the listed applicant for CERAMENT BONE VOID FILLER, MODEL A0210?

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

What is the FDA product code for CERAMENT BONE VOID FILLER, MODEL A0210?

The FDA product code for CERAMENT BONE VOID FILLER, MODEL A0210 is MQV.

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 Bonesupport AB 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.

K234008CERAMENT GK240459Cerament Bone Void FillerK201535Cerament Bone Void FillerK090871CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12K051951CERAMENT BONE VOID FILLER

Related Devices (Code: MQV)

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.

K262230Mg OSTEOREVIVE™;Mg OSTEOCRETE™Bone Solutions, Inc.K260364Device 300419 StripGeistlich Pharma AGK252797JAZBI™ Resorbable Bone Void FillerSdip Innovations Pty, Ltd.K261008Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft SubstituteStryker SpineK253524Adaptos®Fuse Bone GraftBiomendex OYK253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft SubstituteProsidyan, Inc.

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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