Atlas FDA

LB MEDICAL INFLATABLE TISSUE ELEVATOR/EXPANDER SYSTEM

FDA 510(k) clearance K080158 · decided 2008-05-02

Clearance details

K-number
K080158
Device name
LB MEDICAL INFLATABLE TISSUE ELEVATOR/EXPANDER SYSTEM
Applicant
Lb Medical LLC
Decision
Substantially Equivalent
Date received
2008-01-23
Decision date
2008-05-02
Days to decision
100 days
Clearance type
Traditional
Product code
FZW
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Alexandria, VA, 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
BIRCOLL BALLOON DISSECTOR (K984448)Wells Johnson Co.1999-01-28
SPACEMAKER SURGICALBALLOON DISSECTOR/EXPANDER (K972109)General Surgical Innovations1997-11-14
AESCULAP SKIN GRAFT MESHER (K936186)Aesculap, Inc.1994-03-10
INAMED RUIZ-COHEN INTRAOPERATIVE TISSUE EXPANDER (K904265)Inamed Development Co.1991-03-06
SURGITEK INTRA-SPAN INTRAOPERATIVE TISSUE EXPANDER (K902349)Surgitek1990-09-05
MENTOR RAPID-SPAN (TM) TISSUE EXPANDER (K883303)Mentor Corp.1988-08-26
CUI, VERSAFIL(TM), STE(TM) TISSUE EXPANDER (K874276)Cox-Uphuff Intl.1987-12-02

Recalls involving this device

No recalls on record reference this clearance.