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

BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL BMCD-35-3040, MBCD-35-4050

K Number: K014243 · Decision Mar 26, 2002
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
90

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Basic Information

Device Name
BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL BMCD-35-3040, MBCD-35-4050
K Number
K014243
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Triage Medical, Inc.
Date Received
December 26, 2001
Decision Date
March 26, 2002
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

Similar 510(k) Clearances

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

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Other Clearances by Triage Medical, Inc.

K Number Device Name
K062391 DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00
K052043 3.8MM CS FACET COMPRESSION DEVICE
K051949 4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
K043351 4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N; SFCD-45-3040S OR N
K042244 BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE
K040250 BONE-LOK HP WASHER
K014304 BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR, MODEL BMCD-35-3050S
K012817 HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
K012818 HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
K012280 TITANIUM COMPRESSION ANCHOR SYSTEM MODEL VERSION 2
Search all 11 clearances from Triage Medical, Inc. →