510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Kinetikos Medical, Inc.

San Diego, CA, US

Kinetikos Medical, Inc. appears in FDA device records in San Diego, CA. FDA records list 19 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
19
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 19 510(k) clearances for Kinetikos Medical, Inc. between 1994 and 2006. The busiest year on record is 1996, with 5. The most recent is 2006, with 2.

Clearances by year, as a table
510(k) clearance decisions for Kinetikos Medical, Inc., by decision year
YearClearances
19941
19951
19965
19992
20022
20032
20043
20051
20062
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K061749ECLIPSE TOTAL ANKLE IMPLANTHSNSubstantially Equivalent
K061465KMI CEMENT RESTRICTOR IMPLANTJDKUnknown
K051611MBARESORB IMPLANTHWCSubstantially Equivalent
K041461KMI DISTAL VOLAR RADIUS PLATE SYSTEMHRSSubstantially Equivalent
K032806KATALYST RADIAL HEAD IMPLANTKWISubstantially Equivalent
K040356KOMPRESSOR SCREW SYSTEMHWCSubstantially Equivalent
K024233KOMPRESSOR SCREW SYSTEMHWCSubstantially Equivalent
K030037UNIVERSAL TOTAL WRIST SYSTEMJWJSubstantially Equivalent
K023770K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)KWDSubstantially Equivalent
K020554MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEMJWJSubstantially Equivalent
K991873KMI WRIST FUSION SYSTEMHRSSubstantially Equivalent
K990094KMI WRIST FUSION SYSTEMHRSSubstantially Equivalent
K960692SUBTALAR MBA SYSTEMHWCSubstantially Equivalent
K960539DIAO HAND SURGERY SETHXBSubstantially Equivalent
K961051UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)JWJSubstantially Equivalent
K960537K2 BONE SCREW SYSTEMHWCSubstantially Equivalent for Some Indications
K960533K3 BONE SCREW SYSTEMHWCSubstantially Equivalent for Some Indications
K950704K4 BONE SCREW SYSTEMHWCSubstantially Equivalent
K924724KINETIK GREAT TOE SYSTEMLZJSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain