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FDA 510(k)

CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12

K-Number: K090871 · 2009-09-04

ApplicantBonesupport AB
Decision Date2009-09-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 is the device name listed in this FDA 510(k) record. The listed applicant is Bonesupport AB. It received FDA 510(k) clearance on 2009-09-04 under 510(k) number K090871. 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 IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12?

CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 is a medical device that received FDA 510(k) clearance on 2009-09-04. The listed applicant is Bonesupport AB. The 510(k) number is K090871.

When did CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 receive FDA 510(k) clearance?

CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 received FDA 510(k) clearance on 2009-09-04, under 510(k) number K090871.

Who is the listed applicant for CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12?

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 IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12?

The FDA product code for CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 is MQV.

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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 FillerK073316CERAMENT BONE VOID FILLER, MODEL A0210K051951CERAMENT 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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