Atlas FDA

INNOVA TELESCOPIC DISTRACTOR

FDA 510(k) clearance K984117 · decided 1999-02-10

Clearance details

K-number
K984117
Device name
INNOVA TELESCOPIC DISTRACTOR
Applicant
Innova Corp.
Decision
Substantially Equivalent
Date received
1998-11-17
Decision date
1999-02-10
Days to decision
85 days
Clearance type
Traditional
Product code
MQN
Device class
2
Regulation number
872.4760
Medical specialty
Dental
Advisory committee
Dental
Location
Washington, DC, US
Third-party review
No
Expedited review
No

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Mandible External Fixator - MR Conditional (K143285)Synthes USA Products, LLC2015-05-28
STRYKER PEDIATRIC MANDIBLE DISTRACTOR (K133398)Stryker2014-03-20
SYNTHES CURVILINEAR DISTRACTION SYSTEM (K121502)Synthes, Inc.2012-08-23
MIS CREST WIDENER (K080458)Mis - Implant Technologies , Ltd.2008-12-17
DISTRAX (K080542)John W. King2008-12-15
SYNTHES (USA) CURVILINEAR DISTRACTION SYSTEM (K080153)Synthes (Usa)2008-05-14
KLS MARTIN XTERNAL FIXATOR (K072764)KLS Martin L.P.2007-12-20

Recalls involving this device

No recalls on record reference this clearance.