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

MICRO/MINI N-PK(H) BONE ANCHOR

K Number: K121356 · Decision Nov 9, 2012
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
12
Review Days
189

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MICRO/MINI N-PK(H) BONE ANCHOR
K Number
K121356
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Anulex Technologies, Inc.
Date Received
May 4, 2012
Decision Date
November 9, 2012
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

Similar 510(k) Clearances

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

View all

Other Clearances by Anulex Technologies, Inc.

K Number Device Name
K121354 MICRO/MINI N-PK(F) BONE ANCHOR
K113805 FIXATE TISSUE BAND
K113400 FIXATE TISSUE BAND
K112849 FIXATE TISSUE BAND
K111462 FIXATE TISSUE BAND
K100572 VERSACLOSE, MODEL VC-200-01
K091432 XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01
K082729 RIMCLOSE BONE ANCHOR
K062307 XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS
K061386 ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB
Search all 12 clearances from Anulex Technologies, Inc. →