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

REPOSE BONE SCREW SYSTEM

K Number: K981677 · Decision Aug 27, 1999
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
16
Review Days
472

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Basic Information

Device Name
REPOSE BONE SCREW SYSTEM
K Number
K981677
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Influence, Inc.
Date Received
May 12, 1998
Decision Date
August 27, 1999
Product Code
LRK
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
LRK Device, Anti-Snoring

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Other Clearances by Influence, Inc.

K Number Device Name
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
K972622 STRAIGHT-IN BONE SCREW FIXATION SYSTEM
Search all 16 clearances from Influence, Inc. →