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

STERLING INTERFERENCE SCREW ST

K Number: K050767 · Decision Jun 9, 2005
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
76

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Basic Information

Device Name
STERLING INTERFERENCE SCREW ST
K Number
K050767
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Regeneration Technologies, Inc.
Date Received
March 25, 2005
Decision Date
June 9, 2005
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other 510(k) clearances with the same product code (HWC), 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
K051615 STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES
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. →