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

INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM

K Number: K103194 · Decision Apr 21, 2011
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
5
Review Days
174

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Basic Information

Device Name
INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM
K Number
K103194
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intra-Lock International, Inc.
Date Received
October 29, 2010
Decision Date
April 21, 2011
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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

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Other Clearances by Intra-Lock International, Inc.

K Number Device Name
K171831 Intra-Lock Bone Fixation System
K133613 INTRA-LOCK DENTAL IMPLANTS
K111199 INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM 3.4MM IMPLANT ANGLED ABUTMENTS
K082419 REOSS POWDER, REOSS PUTTY, REOSS GEL, MODELS R-1,RP-1, RG-1