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

BIOSPHERE SUTURE ANCHOR

K Number: K963396 · Decision May 6, 1997
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
28
Review Days
251

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Basic Information

Device Name
BIOSPHERE SUTURE ANCHOR
K Number
K963396
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Instrument Makar, Inc.
Date Received
August 28, 1996
Decision Date
May 6, 1997
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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Other Clearances by Instrument Makar, Inc.

K Number Device Name
K002600 LITWIN CRUICATE ANCHOR
K980999 ST LEGER CEMENTED SEMI-CONSTRAINED TOTAL KNEE IMPLANT
K964364 DISPOSABLE APRON
K955835 FLUID BARRIER BOOT KNEE & ANKLE-HIGH
K960555 BIOASBSORBABLE MINI-SCREW SUTURE ANCHOR
K943249 BIOABSORBABLE INTERFERENCE SCREW
K942828 MAKAR FULL AND HALF FACE SHIELD
K944062 LAPRASCOPIC GRASPER
K930980 INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW
K923841 BONE SCREWS
Search all 28 clearances from Instrument Makar, Inc. →