Atlas FDA

ADD-ON CONDYLE

FDA 510(k) clearance K002790 · decided 2001-08-06

Clearance details

K-number
K002790
Device name
ADD-ON CONDYLE
Applicant
Walter Lorenz Surgical, Inc.
Decision
Substantially Equivalent
Date received
2000-09-07
Decision date
2001-08-06
Days to decision
333 days
Clearance type
Traditional
Product code
NEI
Device class
2
Regulation number
872.4770
Medical specialty
Dental
Advisory committee
Dental
Location
Jacksonville, FL, 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
STRYKER TEMPORARY CONDYLAR PROSTHESIS (K133285)Stryker2014-04-09
MODIFICATION TO SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM (K081747)Synthes (Usa)2008-09-05
SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM (K063181)Synthes (Usa)2007-01-05
OSTEOMED TEMPORARY CONDYLAR ATTACHMENT SYSTEM (K031701)Osteomed LP2004-07-08
KLS-MARTIN TEMPORARY CONDYLAR IMPLANT (K990667)KLS-Martin L.P.2001-07-27
SYNTHES LOCKING RECONSTRUCTION PLATE (LRP) WITH CONDYLAR HEAD (K990637)Synthes (Usa)1999-10-22

Recalls involving this device

No recalls on record reference this clearance.