Atlas FDA

WRIGHT DOW CORNING SOFTGOODS W/DOW

FDA 510(k) clearance K792269 · decided 1980-02-05

Clearance details

K-number
K792269
Device name
WRIGHT DOW CORNING SOFTGOODS W/DOW
Applicant
Dow Corning Wright
Decision
Substantially Equivalent
Date received
1979-11-09
Decision date
1980-02-05
Days to decision
88 days
Clearance type
Traditional
Product code
IPY
Device class
1
Regulation number
890.3490
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
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
M-BRACE (K823882)Buckman Consultants1983-01-17
LUMBOSACRAL SUPPORT (K823823)Danek Medical, Inc.1983-01-14
CUSTOM CONTOUR LUMBOSACRAL ORTHOSIS (K812422)Surgical Appliance Industries, Inc.1981-09-14
CASH ORTHOSIS (K812099)David Hendricks, C.P.O.1981-08-13
LUMBO-SACRAL FLEXION ORTHOSIS (K811494)Surgical Appliance Industries, Inc.1981-06-16
LUMBAR FLEXION BRACE (K810554)Orthomedics1981-03-13
SPINAL EXTENSION BRACE (K810556)Orthomedics1981-03-13
CRUSADER HYPEREXTENSION BRACE (K803033)Orthomedics1980-12-22
LUMBOSACRAL SUPPORTS & THORACO-LUMBO-SAC (K801712)Fred Sammons, Inc.1980-08-07
VERTEBRACE SPINAL SUPPORTS (K791314)Vertebrace, Inc.1979-07-30

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS (P880076/S001)Dow Corning Wright1991-06-17