Atlas FDA

OSTEOMED GREAT TOE SYSTEM

FDA 510(k) clearance K922211 · decided 1993-11-09

Clearance details

K-number
K922211
Device name
OSTEOMED GREAT TOE SYSTEM
Applicant
Osteomed Corp.
Decision
Substantially Equivalent for Some Indications
Date received
1992-05-12
Decision date
1993-11-09
Days to decision
546 days
Clearance type
Traditional
Product code
LZJ
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Glendale, CA, 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
ARTHROSURFACE TOEMOTION (K132496)Arthrosurface, Inc.2014-02-26
THE ASCENSION MOVEMENT GREAT TOE SYSTEM TOTAL ARTHROPLASTY (K102549)Ascension Orthopedics, Inc.2010-12-21
MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM (K072251)Merete Medical GmbH2008-05-08
GTS GREAT TOE SYSTEM - (METATARSAL COMPONENT WITH POROUS COATING) (K950864)Acu Med, Inc.1995-07-31
TOTAL TOE SYSTEM II (K941650)Biomet, Inc.1994-12-19
KINETIK GREAT TOE SYSTEM (K924724)Kinetikos Medical, Inc.1994-01-05
TOTAL TOE SYSTEM (K920446)Biomet, Inc.1993-03-22
GREAT TOE IMPLANT (K920667)Acu Med, Inc.1992-06-19
ANATOMIC TOE SYSTEM (K911552)Orthopaedic Biosystems1991-06-28
KOENIG TOTAL TOE IMPLANT (K884561)Dow Corning Wright1989-01-24

Recalls involving this device

No recalls on record reference this clearance.