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

CAPSET CALCIUM SULFATE BONE GRAFT PLASTER

K Number: K955096 · Decision Jan 23, 1996
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
34
Review Days
77

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Basic Information

Device Name
CAPSET CALCIUM SULFATE BONE GRAFT PLASTER
K Number
K955096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lifecore Biomedical, Inc.
Date Received
November 7, 1995
Decision Date
January 23, 1996
Product Code
LYC
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
LYC Bone Grafting Material, Synthetic

Similar 510(k) Clearances

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

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Other Clearances by Lifecore Biomedical, Inc.

K Number Device Name
K073032 PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTS
K072241 PRIMACONNEX CAD/CAM ABUTMENT SYSTEM
K072768 RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTS
K072572 PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS
K062876 PRIMACONNEX CERAMIC ABUTMENTS
K060530 SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
K053643 STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026
K051614 PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS
K050506 PRIMASOLO ONE-PIECE IMPLANTS & HEALING CAPS
K041324 CALMATRIX CALCIUM SULFATE BONE GRAFT BINDER
Search all 34 clearances from Lifecore Biomedical, Inc. →