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

STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM

K Number: K990095 · Decision Feb 1, 1999
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
16
Review Days
20

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Basic Information

Device Name
STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM
K Number
K990095
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 12, 1999
Decision Date
February 1, 1999
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

Similar 510(k) Clearances

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

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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
K983325 IN-PROBE II URODYNAMIC SYSTEM
K982155 SHORT STRAIGHT-IN BONE SCREW FIXATION SYSTEM
K981631 INFLUENCE CLIP SYSTEM
K980482 TRIANGLE SLING
K972622 STRAIGHT-IN BONE SCREW FIXATION SYSTEM
Search all 16 clearances from Influence, Inc. →