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FDA 510(k)

AFT ALLOGRAFT FILLER TUBE

K-Number: K060161 · 2006-03-21

ApplicantMusculoskeletal Transplant Foundation
Decision Date2006-03-21
Product CodeMBP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AFT ALLOGRAFT FILLER TUBE 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 2006-03-21 under 510(k) number K060161. The device is classified under product code MBP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFT ALLOGRAFT FILLER TUBE?

AFT ALLOGRAFT FILLER TUBE is a medical device that received FDA 510(k) clearance on 2006-03-21. The listed applicant is Musculoskeletal Transplant Foundation. The 510(k) number is K060161.

When did AFT ALLOGRAFT FILLER TUBE receive FDA 510(k) clearance?

AFT ALLOGRAFT FILLER TUBE received FDA 510(k) clearance on 2006-03-21, under 510(k) number K060161.

Who is the listed applicant for AFT ALLOGRAFT FILLER TUBE?

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 AFT ALLOGRAFT FILLER TUBE?

The FDA product code for AFT ALLOGRAFT FILLER TUBE is MBP.

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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 FILLERK110003MTF NEW BONE VOID FILLERK103784DBX DEMINERALIZED BONE MATRIX PUTTY

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Related Devices (Code: MBP)

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.

K242799PliaFX FloLifenet HealthK130703VIVORTE BVFVivorte, Inc.K130498OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTYBacterin International, Inc.K122513CLEARED UNDER GRAFTON II EDBMMedtronic Sofamor Danek, Inc.K113728SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTYHans Biomed Corp.K103742ACCELL EVO3 (FORMERLY ACCELL A2I)Integra Life Sciences

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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