Atlas FDA

JURGAN PIN BALL

FDA 510(k) clearance K831072 · decided 1983-06-08

Clearance details

K-number
K831072
Device name
JURGAN PIN BALL
Applicant
Jurgan Development & Mfg., Ltd.
Decision
Substantially Equivalent
Date received
1983-04-04
Decision date
1983-06-08
Days to decision
65 days
Clearance type
Traditional
Product code
LYT
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Walker, MI, 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
CERAMIC TIPPED SKULL PIN (K040363)The Jerome Group, Inc.2004-04-12
BONE BAND (K983685)Chapel and Assoc.1998-12-04
OSTEONICS FX-CABLELOK GRIP COMPONENTS (K980594)Osteonics Corp.1998-05-05
K-CAP-E, STERILE (K914812)Westcon Orthopedics, Inc.1992-01-09
K-CAP-I, STERILE (K912762)Westcon Orthopedics, Inc.1991-07-18
MICROGUARD, ORTHOPEDIC PIN PROTECTORS (K902676)Micro-Aire Surgical Instruments, Inc.1990-09-14
K-CAP-I ORTHOPEDIC FIXATION WIRE CAP (K902053)Westcon Orthopedics, Inc.1990-09-14
HORIZON ORTHOPEDIC PIN PROTECTOR (K883576)Horizon Medical, Inc.1988-09-30

Recalls involving this device

No recalls on record reference this clearance.