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

STRAUMANN GRANULES

K Number: K040646 · Decision May 3, 2004
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
14
Review Days
53

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
STRAUMANN GRANULES
K Number
K040646
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Straumann Co.
Date Received
March 11, 2004
Decision Date
May 3, 2004
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.

View all

Other Clearances by The Straumann Co.

K Number Device Name
K041070 STRAUMANN TEMPORARY COPING
K040469 THE STRAUMANN ORTHO IMPLANT SYSTEM
K993862 MODUS SAGITTAL SPLIT PLATE
K962023 PLASTIC PROTECTION HEALING CAPS
K960634 TITANIUM HEALING CAPS
K955281 ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
K955369 MEMFIX
K941393 ITI ANGLED ABUTMENT
K943720 ITI TRANSVERSAL SCREWING SYSTEM
K931993 ITI DISTANCE SYSTEM
Search all 14 clearances from The Straumann Co. →