Atlas FDA

VERTETRAC

FDA 510(k) clearance K771988 · decided 1979-02-01

Clearance details

K-number
K771988
Device name
VERTETRAC
Applicant
Ballert Orthopedic Corp.
Decision
Substantially Equivalent
Date received
1977-10-19
Decision date
1979-02-01
Days to decision
470 days
Clearance type
Traditional
Product code
HST
Device class
1
Regulation number
888.5850
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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BACK-ON-TRAC, MODEL 101BOT (K984190)Back-On-Track, Inc.1999-03-15
K AND D HOME TRACT (K872121)Joseph A. Kott, M.D.1987-08-12
ARTHROSCOPIC SHOULDER HOLDER (K870212)Dyonics, Inc.1987-02-20
EXTREMITY ELEVATOR (K870125)Orthopedic Systems, Inc.1987-02-04
TUPPER TROLLEY (K870102)Orthopedic Systems, Inc.1987-02-03
MODEL 668, TRACTION SPLINT, ADULT (K864765)Ferno-Washington, Inc.1986-12-17
THE TOWERED 90/90 UNIT (K862874)Lossing Orthopedic, Inc.1986-08-07
TRANSFER-TRAX (TM) SPLINT TRACTION (K855179)Comfortex, Inc.1986-01-21
SUSPENDER ORTHOPEDIC SUSPENSION DEVICE (K860037)Comfortex, Inc.1986-01-21
NEC-KRADLE BY VENCOR (K844239)Vencor1984-11-19

Recalls involving this device

No recalls on record reference this clearance.