Atlas FDA

HIP ABDUCTION SPLINT

FDA 510(k) clearance K810557 · decided 1981-03-13

Clearance details

K-number
K810557
Device name
HIP ABDUCTION SPLINT
Applicant
Orthomedics
Decision
Substantially Equivalent
Date received
1981-03-02
Decision date
1981-03-13
Days to decision
11 days
Clearance type
Traditional
Product code
IOZ
Device class
1
Regulation number
890.3665
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
ABDUCTION PILLOW (K830243)Warm & Form, Orthopedic Materials1983-03-08
ABDUCTION PILLOW (K823820)Danek Medical, Inc.1983-01-14
PAVLIK HARNESS (K780375)Biomet, Inc.1978-03-15

Recalls involving this device

No recalls on record reference this clearance.