Atlas FDA

SPLINT, BOHLER

FDA 510(k) clearance K770612 · decided 1977-04-08

Clearance details

K-number
K770612
Device name
SPLINT, BOHLER
Applicant
Will Ross Co.
Decision
Substantially Equivalent
Date received
1977-03-31
Decision date
1977-04-08
Days to decision
8 days
Clearance type
Traditional
Product code
IQI
Device class
1
Regulation number
890.3475
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Mchenry, IL, 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
Neurosplint (K143458)Neurospectrum, LLC2015-08-13
SENSOR WALK (K052771)Otto Bock Healthcare LP2006-05-03
SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1 (K031576)Surgitech, Inc.2003-07-31
ACCUFLEX DYNAMIC ELBOW ORTHOSIS (K926391)Regulatory & Marketing Services, Inc.1993-07-22
MCCONNELL SHOULDER BRACE (K910974)Mcconnell Orthopedic1991-03-21
GAIT-AID ORTHOPEDIC INSOLE (K874502)Gait-Aid, Inc.1987-11-30
ADJUSTABLE POLYCENTRIC ELBOW HINGE (K831542)Fred Sammons, Inc.1983-06-24
DROP FOOT BRACE (K831615)Edward Dilauro, Jr.1983-06-15
VARIOUS SUPPORTS AND SPLINTS (K823812)Danek Medical, Inc.1983-01-14
BRACE-UP ALL PURPOSE WRIST BAND (K823113)Arco Matic, Inc.1982-11-16
ROTATION BOOT (K823160)Warm & Form, Orthopedic Materials1982-11-10
BRACE-UP STOCKING KNEE BRACE (K823114)Arco Matic, Inc.1982-11-05

Recalls involving this device

No recalls on record reference this clearance.