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Wax, Bone

FDA product code MTJ · Class U · Unknown

46
Registered devices
233
Adverse events
4
Recalls
42
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-12-06Baxter Healthcare CorporationCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align wi
2012-07-05Synthes USA HQ, Inc.There is the potential for Hemostatic Bone Putty to ignite if contacted with electrosurgical cautery systems under certain conditions during surgery.
2012-01-06Synthes, Inc.Revision A of the Hemostatic Bone Putty Brochure (J10847A) was sent to sales consultants instead of Revision B (J10847B), which corrected an error in the indica
2008-10-28Ethicon, Inc.A hospital reported to their Ethicon sales representative that they had an "unmarked" box of bone was on their shipping dock that they could not receive due to

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.