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

BONE GRAFT SCREW SYSTEM

K Number: K973056 · Decision Nov 12, 1997
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
13
Review Days
89

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Basic Information

Device Name
BONE GRAFT SCREW SYSTEM
K Number
K973056
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bicon, Inc.
Date Received
August 15, 1997
Decision Date
November 12, 1997
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZL), ordered by most recent decision date.

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Other Clearances by Bicon, Inc.

K Number Device Name
K062044 THE 5.0 X 6.0MM DENTAL IMPLANT
K051091 SYNTHOGRAFT
K050712 4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT
K050408 BICON ORTHODONTIC IMPLANT SYSTEM
K031568 BICONITE SURFACE TREATMENT
K042637 THE 5.0 X 6.0MM DENTAL IMPLANT
K023705 BICON TRANSITIONAL IMPLANT (BTI) SYSTEM
K010185 6.0 X 5.7MM DENTAL IMPLANT
K994037 THE 4.5MM DIAMETER BICON DENTAL IMPLANT
K982488 BICON BONE SCREW SYSTEM
Search all 13 clearances from Bicon, Inc. →