Atlas FDA

ACE SYSTEM

FDA 510(k) clearance K960853 · decided 1996-04-03

Clearance details

K-number
K960853
Device name
ACE SYSTEM
Applicant
Xomed, Inc.
Decision
Substantially Equivalent
Date received
1996-03-01
Decision date
1996-04-03
Days to decision
33 days
Clearance type
Traditional
Product code
EQJ
Device class
1
Regulation number
874.4140
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Jacksonville, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Precision Thin Reciprocating Blade, 0.010in. (K161514)Stryker Corporation2017-01-17
XPS CURVED BUR (K041985)Medtronic Xomed, Inc.2004-08-12
ESSENTIAL SHAVER SYSTEM (K974232)Gyrus Ent LLC1998-01-12
TREBAY MICRODEBRIDER SYSTEM (K955704)Trebay Medical Corp.1996-01-30
SOF - ABRASION BUR (K955294)Trebay Medical Corp.1995-12-22
TREBAY IRRIGATED CUTTER BLADE (MODIFICATION) (K954912)Trebay Medical Corp.1995-12-06
KARL STORZ ENT SHAVER (K953370)KARL STORZ Endoscopy-America, Inc.1995-09-06
KARL STORZ STAMMBERGER-SACHSE INTRANASAL-FRILL (K950337)KARL STORZ Endoscopy-America, Inc.1995-08-23
REDI DRILL DRILL SYSTEM (K952609)Trebay Medical Corp.1995-07-31
ESSENTIAL SHAVER SYSTEM (K953096)Smith & Nephew Richards, Inc.1995-07-28
KARL STORZ MICRO-INSTRUMENT FOR COCHLEAR IMPLANTATION (K946332)KARL STORZ Endoscopy-America, Inc.1995-06-05
TREBAY IRRGATED CUTTER BLADE (K951526)Trebay Medical Corp.1995-05-12

Recalls involving this device

No recalls on record reference this clearance.