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

STERNGOLD U-CPF METAL ALLOY (1067800)

K Number: K962324 · Decision Jul 24, 1996
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
193
Applicant Total
16
Review Days
37

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Basic Information

Device Name
STERNGOLD U-CPF METAL ALLOY (1067800)
K Number
K962324
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sterngold/Implamed
Date Received
June 17, 1996
Decision Date
July 24, 1996
Product Code
EJS
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
EJS Alloy, Other Noble Metal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EJS), 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
K983786 STERNGOLD IMPLAMED WIDE PLATFORM DENTAL IMPLANTS AND RELATED PROSTHETICS AND INSTTUMENTATION
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)
K962325 QUASAR YELLOW CROWN AND BRIDGE ALLOY (1122015)
K962304 STERNGOLD BIO-4
K962303 STERNGOLD CF
Search all 16 clearances from Sterngold/Implamed →