Atlas FDA

PLASTER TABLE 1418

FDA 510(k) clearance K873274 · decided 1987-09-17

Clearance details

K-number
K873274
Device name
PLASTER TABLE 1418
Applicant
Stierlen-Maquet AG
Decision
Substantially Equivalent
Date received
1987-08-17
Decision date
1987-09-17
Days to decision
31 days
Clearance type
Traditional
Product code
JEB
Device class
1
Regulation number
878.4950
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
West Germany, GR
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
ORTHOVISION TABLE (K905816)American Sterilizer Co.1991-03-06
SCHOLTEN FRAME (K900405)Scholten Surgical Instruments, Inc.1990-03-01
ORTHO-J, INC. BEK-JS-004 (K891917)Ortho-J, Inc.1989-05-26
WILLIAMS BELT & BOOT (K891387)Arthro-Medic, Inc.1989-05-23
K ORTHOPEDIC TABLE (K881101)Instrumentation Specialties, Inc.1988-04-06
OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION (K880263)Orthopedic Systems, Inc.1988-03-15
EXTENSION DEVICE 1416 (K873276)Stierlen-Maquet AG1987-09-17
EXTENSION TABLE 1417 (K873275)Stierlen-Maquet AG1987-09-17
ORTHOPAEDIC TABLE 1420 (K873273)Stierlen-Maquet AG1987-09-17
CAST BLOCK (K781082)Orthopedic Equipment Co., Inc.1978-07-07
ARTHROSTRESS (K772321)Mtd, Inc.1978-01-03
SPINAL SURGERY FRAME (K771020)Orthopedic Systems, Inc.1977-06-17

Recalls involving this device

No recalls on record reference this clearance.