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FDA 510(k)

MTF NEW BONE VOID FILLER

K-Number: K110003 · 2011-10-13

ApplicantMusculoskeletal Transplant Foundation
Decision Date2011-10-13
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MTF NEW BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Musculoskeletal Transplant Foundation. It received FDA 510(k) clearance on 2011-10-13 under 510(k) number K110003. 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 MTF NEW BONE VOID FILLER?

MTF NEW BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2011-10-13. The listed applicant is Musculoskeletal Transplant Foundation. The 510(k) number is K110003.

When did MTF NEW BONE VOID FILLER receive FDA 510(k) clearance?

MTF NEW BONE VOID FILLER received FDA 510(k) clearance on 2011-10-13, under 510(k) number K110003.

Who is the listed applicant for MTF NEW BONE VOID FILLER?

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

What is the FDA product code for MTF NEW BONE VOID FILLER?

The FDA product code for MTF NEW BONE VOID FILLER is MQV.

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Other records listing Musculoskeletal Transplant Foundation 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.

K181633MTF Pre-Sutured TendonK121313MTF NEW BONE VOID FILLERK120479MTF FASCIAK113167MTF NEW BONE VOILD FILLERK103795DBX DEMINERALIZED BONE MATRIX PUTTYK103784DBX DEMINERALIZED BONE MATRIX PUTTY

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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

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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