FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DBX DEMINERALIZED BONE MATRIX PUTTY

K Number: K091217 · Decision Oct 2, 2009
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
14
Applicant Total
24
Review Days
158

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DBX DEMINERALIZED BONE MATRIX PUTTY
K Number
K091217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Musculoskeletal Transplant Foundation
Date Received
April 27, 2009
Decision Date
October 2, 2009
Product Code
NUN
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NUN Bone Grafting Material, Human Source

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NUN), ordered by most recent decision date.

View all

Other Clearances by Musculoskeletal Transplant Foundation

K Number Device Name
K181633 MTF Pre-Sutured Tendon
K121313 MTF NEW BONE VOID FILLER
K120479 MTF FASCIA
K113167 MTF NEW BONE VOILD FILLER
K110003 MTF NEW BONE VOID FILLER
K103795 DBX DEMINERALIZED BONE MATRIX PUTTY
K103784 DBX DEMINERALIZED BONE MATRIX PUTTY
K091218 DBX DEMINERALIZED BONE MATRIX PUTTY
K080399 DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
K080405 SYGNAL DBM
Search all 24 clearances from Musculoskeletal Transplant Foundation →