Atlas FDA

SKYTRON MODEL 130 SURGICAL TABLE

FDA 510(k) clearance K873478 · decided 1987-09-24

Clearance details

K-number
K873478
Device name
SKYTRON MODEL 130 SURGICAL TABLE
Applicant
Skytron, Div. the Kmw Group, Inc.
Decision
Substantially Equivalent
Date received
1987-08-24
Decision date
1987-09-24
Days to decision
31 days
Clearance type
Traditional
Product code
FWY
Device class
1
Regulation number
878.4950
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Grand Rapids, 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
ASST-3000 SPINAL SURGERY TABLE (K883457)Orthopedic Systems, Inc.1988-08-26
CHEMONUCLEOLYSIS TABLE (K833509)Stryker Corp.1983-11-28
CHICK SURGICAL TABLE (K800118)Warner-Lambert Co.1980-02-05

Recalls involving this device

No recalls on record reference this clearance.