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

STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND INSTTUMENTATION

K Number: K983786 · Decision Nov 13, 1998
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
16
Review Days
17

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Basic Information

Device Name
STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND INSTTUMENTATION
K Number
K983786
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sterngold/Implamed
Date Received
October 27, 1998
Decision Date
November 13, 1998
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 Sterngold/Implamed

K Number Device Name
K984341 STERNVANTAGE VARNISH LC, MODEL 221001
K984340 STERNOMEGA TEMPORARY CEMENT AUTOMIX NE, MODEL 220282/220281
K982692 STERNOMEGA BONDING AGENT, STERNOMEGA COMPOSITE LC, STERNOMEGA COMPOMER LC
K982895 STERNOMEGA COMPOMER CEMENT
K981516 STERNGOLD IMPLAMED HEX SCREW IMPLANT TPS COATED STERNGOLD IMPLAMED HEX SCREW IMPLANT HA COATED , REFER TO TABLE 1 IN SUB
K962326 STERNGOLD BIO-5 (1127210)
K962324 STERNGOLD U-CPF METAL ALLOY (1067800)
K962325 QUASAR YELLOW CROWN AND BRIDGE ALLOY (1122015)
K962304 STERNGOLD BIO-4
K962303 STERNGOLD CF
Search all 16 clearances from Sterngold/Implamed →