Atlas FDA

THE DENVER SPLINT

FDA 510(k) clearance K791681 · decided 1979-10-22

Clearance details

K-number
K791681
Device name
THE DENVER SPLINT
Applicant
Xomed, Inc.
Decision
Substantially Equivalent
Date received
1979-08-28
Decision date
1979-10-22
Days to decision
55 days
Clearance type
Traditional
Product code
EPP
Device class
1
Regulation number
874.5800
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Arnold, MO, 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
AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS (K942158)Wfr/Aquaplast Corp.1994-07-29
EXTERNAL NASAL SPLINT (K942724)Micromed Development Corp.1994-07-08
MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT (K895502)Microbio-Medics, Inc.1989-12-08
HOOD NASAL SPLINT (K890599)Hood Laboratories1989-03-17
RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT (K882244)Richards Medical Co., Inc.1988-06-23
AMERICAN NASAL SPONGE (K872905)American Silk Sutures, Inc.1987-09-04
'EXMOOR' ATKINS NASAL SPLINT (K864930)Exmoor Plastics , Ltd.1987-03-04
'EXMOOR' SHAH & MACKAY NASAL SPLINTS (K864933)Exmoor Plastics , Ltd.1987-03-04
'EXMOOR' CAWOOD NASAL SPLINTS (K864932)Exmoor Plastics , Ltd.1987-03-04
'EXMOOR' SHAH SILICONE DISCS (K864934)Exmoor Plastics , Ltd.1987-01-28
CANNON NASAL SPLINT (K863382)Treace Medical, Inc.1986-10-07
MICROTEK INTRANASAL SPLINT (K862496)Microtek Medical, Inc.1986-07-14

Recalls involving this device

No recalls on record reference this clearance.