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Musculoskeletal Transplant Foundation, Inc.

7 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void fil recall (Z-1066-2024)Musculoskeletal Transplant Foundation, Inc.2024-02-09
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void fil recall (Z-1067-2024)Musculoskeletal Transplant Foundation, Inc.2024-02-09
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created oss recall (Z-0323-2024)Musculoskeletal Transplant Foundation, Inc.2023-11-17
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treat recall (Z-2004-2016)Musculoskeletal Transplant Foundation, Inc.2016-06-16
Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze. recall (Z-2210-2015)Musculoskeletal Transplant Foundation, Inc.2015-07-24
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are d recall (Z-2075-2015)Musculoskeletal Transplant Foundation, Inc.2015-07-15
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler. recall (Z-1455-2015)Musculoskeletal Transplant Foundation, Inc.2015-04-17

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Every clearance here is in the API, with alerts when new ones post.