DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX
K-Number: K040501 · 2005-04-29
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Device Summary
Frequently Asked Questions
What is the DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX?
DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX is a medical device that received FDA 510(k) clearance on 2005-04-29. The listed applicant is Musculoskeletal Transplant Foundation. The 510(k) number is K040501.
When did DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX receive FDA 510(k) clearance?
DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX received FDA 510(k) clearance on 2005-04-29, under 510(k) number K040501.
Who is the listed applicant for DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX?
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 DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX?
The FDA product code for DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX is NUN.
Related Clinical Trials
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.
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.
Related Devices (Code: NUN)
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.
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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