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

STERI-OSS IMMEDIATE PLACEMENT IMPLANT

K Number: K952917 · Decision Oct 16, 1995
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
46
Review Days
112

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Basic Information

Device Name
STERI-OSS IMMEDIATE PLACEMENT IMPLANT
K Number
K952917
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Steri-Oss, Inc.
Date Received
June 26, 1995
Decision Date
October 16, 1995
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 Steri-Oss, Inc.

K Number Device Name
K982400 STERI-OSS' IMPROV TEMPORARY DENTAL CEMENT
K980439 REPLACE CYLINDRICAL IMPLANTS
K973423 STERI-OSS 3.25 MM REPLACE(HYDROXYAPATITE-COATED)DENTAL IMPLANT
K973433 STERI-OSS 3.25 MM REPLACE(TITANIUM PLASMA SPRAYED) 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. →