Atlas FDA

SEPTUM ELEVATOR

FDA 510(k) clearance K890365 · decided 1989-02-03

Clearance details

K-number
K890365
Device name
SEPTUM ELEVATOR
Applicant
Kinetic Medical Products
Decision
Substantially Equivalent
Date received
1989-01-23
Decision date
1989-02-03
Days to decision
11 days
Clearance type
Traditional
Product code
GEG
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Erie, PA, 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
ELEVATORS, VARIOUS TYPES (K891899)Zinnanti Surgical Instruments, Inc.1989-04-12
ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE (K891894)Zinnanti Surgical Instruments, Inc.1989-04-12
SURGICAL ELEVATOR (K890253)Kinetic Medical Products1989-01-27
LIGATURE NEEDLES (K890230)Kinetic Medical Products1989-01-27
1.1 TWIST DRILLS AND 1.2 CORTICAL DRILLS (K872491)Micro-Aire Surgical Instruments, Inc.1987-07-16
ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS (K870781)Buckman Co., Inc.1987-03-09
ELEVATOR, COBB SPINAL (K870591)Military Engineering, Inc.1987-02-26
FEMUR WRENCH (K870126)Orthopedic Systems, Inc.1987-02-03
RAYLOR(TM) PERIOSTEAL ELEVATORS (K864421)Cedar Surgical, Inc.1986-11-26
H.R. JAKOBI SURG. INSTRUMENTS 40/41 (K834176)Imm Enterprises , Ltd.1984-01-27
HARRINGTON SPINAL ELEVATOR (K781449)Orthopedic Equipment Co., Inc.1978-09-27

Recalls involving this device

No recalls on record reference this clearance.