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

STERI-OSS DUAL COATED CYLINDRICAL IMPLANTS

K Number: K911593 · Decision Oct 7, 1993
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
46
Review Days
912

Basic Information

Device Name
STERI-OSS DUAL COATED CYLINDRICAL IMPLANTS
K Number
K911593
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
STERI-OSS, INC.
Date Received
April 9, 1991
Decision Date
October 7, 1993
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

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Other Clearances by STERI-OSS, INC.

K Number Device Name
K982400 STERI-OSS' IMPROV TEMPORARY DENTAL CEMENT
K980439 REPLACE CYLINDRICAL IMPLANTS
K973433 STERI-OSS 3.25 MM REPLACE(TITANIUM PLASMA SPRAYED) DENTAL IMPLANT
K973423 STERI-OSS 3.25 MM REPLACE(HYDROXYAPATITE-COATED)DENTAL IMPLANT
K973402 STERI-OSS 3.25 MM REPLACE DENTAL IMPLANT SYSTEM
K972965 STERI-OSS UNTIL IMPLANT CEMENT
K970073 BIO-ESTHETIC INDIRECT ABUTMENT
K964739 STERI-OSS TIODIZED SCREW
K964220 REPLACE TITANIUM IMPLANT SYSTEM
K963945 STERI-OSS GOLD ATTACHMENT SYSTEM
Search all 46 clearances from STERI-OSS, INC. →