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

IN-FAST BONE SCREW SYSTEM/IN-FAST BONE SCREW INSERTER/IN-FAST BONE SCREW

K Number: K970292 · Decision Apr 23, 1997
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
16
Review Days
89

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Basic Information

Device Name
IN-FAST BONE SCREW SYSTEM/IN-FAST BONE SCREW INSERTER/IN-FAST BONE SCREW
K Number
K970292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Influence, Inc.
Date Received
January 24, 1997
Decision Date
April 23, 1997
Product Code
MBI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by Influence, Inc.

K Number Device Name
K981677 REPOSE BONE SCREW SYSTEM
K991792 CRYO-MONO CRYOGENIC SYSTEM, MODEL CRYO-MONO WITH TUF PROBE
K992277 STAPLETAC BONE ANCHOR SYSTEM
K991122 CRYO-MONO CRYOGRNIC SYSTEM
K990160 MICROTAC-BONE ANCHOR SYSTEM
K990095 STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM
K983325 IN-PROBE II URODYNAMIC SYSTEM
K982155 SHORT STRAIGHT-IN BONE SCREW FIXATION SYSTEM
K981631 INFLUENCE CLIP SYSTEM
K980482 TRIANGLE SLING
Search all 16 clearances from Influence, Inc. →