FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

STERI-OSS SINUS AUGMENTATION KIT

K Number: K963897 · Decision Nov 6, 1996
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
3
Applicant Total
46
Review Days
40

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Basic Information

Device Name
STERI-OSS SINUS AUGMENTATION KIT
K Number
K963897
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Steri-Oss, Inc.
Date Received
September 27, 1996
Decision Date
November 6, 1996
Product Code
EMM
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
EMM Chisel, Osteotome, Surgical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EMM), 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. →