FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES

K Number: K051615 · Decision Aug 15, 2005
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
11
Review Days
59

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Basic Information

Device Name
STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES
K Number
K051615
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Regeneration Technologies, Inc.
Date Received
June 17, 2005
Decision Date
August 15, 2005
Product Code
MQV
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQV Filler, Bone Void, Calcium Compound

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQV), ordered by most recent decision date.

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Other Clearances by Regeneration Technologies, Inc.

K Number Device Name
K080418 REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST
K072238 BIOSET XCH
K072327 CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON
K063584 STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937
K060180 BIOSET XC
K060253 STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.
K052405 STERLING INTERFERENC SCREW HT
K050767 STERLING INTERFERENCE SCREW ST
K043421 OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC
K043420 OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE
Search all 11 clearances from Regeneration Technologies, Inc. →