Atlas FDA

OTI BONE CEMENT PLUG

FDA 510(k) clearance K030608 · decided 2003-06-12

Clearance details

K-number
K030608
Device name
OTI BONE CEMENT PLUG
Applicant
Osteoimplant Technology, Inc.
Decision
Unknown
Date received
2003-02-26
Decision date
2003-06-12
Days to decision
106 days
Clearance type
Traditional
Product code
JDK
Device class
2
Regulation number
878.3300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Hunt Valley, MD, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
VariLift Bone Plug w/ End Cap; 14mm Dia, 24mm long; Ref #: CEA1-14-24-BP; Sterile; Encore recall (Z-0306-2008)Encore Medical, Lp2008-01-09
VariLift Bone Plug w/ End Cap; 16mm Dia, 24mm long; Ref #: CEA1-16-24-BP; Sterile; Encore recall (Z-0307-2008)Encore Medical, Lp2008-01-09
VariLift Bone Plug w/ End Cap; 18mm Dia, 24mm long; Ref #: CEA1-18-24-BP; Sterile; Encore recall (Z-0308-2008)Encore Medical, Lp2008-01-09
VariLift Bone Plug w/ End Cap; 11mm Dia, 24mm long; Ref #: CIE1-11-24-BP; Sterile; Encore recall (Z-0309-2008)Encore Medical, Lp2008-01-09
VariLift Bone Plug w/ End Cap; 13mm Dia, 24mm long; Ref #: CIE1-13-24-BP; Sterile; Encore recall (Z-0310-2008)Encore Medical, Lp2008-01-09
VariLift Bone Plug w/ End Cap; 15mm Dia, 24mm long; Ref #: CIE1-15-24-BP; Sterile; Encore recall (Z-0311-2008)Encore Medical, Lp2008-01-09