ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES

Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

ALLIANCE MEDICAL CORP.

The following data is part of a premarket notification filed by Alliance Medical Corp. with the FDA for Alliance Medical Corporation Reprocessed External Fixation Devices.

Pre-market Notification Details

Device IDK052062
510k NumberK052062
Device Name:ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
ClassificationAppliance, Fixation, Nail/blade/plate Combination, Multiple Component
Applicant ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. Phoenix,  AZ  85044
ContactMoira Barton
CorrespondentMoira Barton
ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. Phoenix,  AZ  85044
Product CodeKTT  
CFR Regulation Number888.3030 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2005-07-29
Decision Date2005-08-25
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00885825019594 K052062 000
00885825019433 K052062 000
00885825019426 K052062 000
00885825019419 K052062 000
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00885825019440 K052062 000
00885825019457 K052062 000
00885825019587 K052062 000
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00885825019563 K052062 000
00885825019556 K052062 000
00885825019549 K052062 000
00885825019532 K052062 000
00885825019525 K052062 000
00885825019518 K052062 000
00885825019501 K052062 000
00885825019495 K052062 000
00885825019488 K052062 000
00885825019471 K052062 000
00885825019464 K052062 000
00885825019303 K052062 000

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