FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CALMPS: BONE, MASTIN, LEWIN, BRAND

K Number: K930028 · Decision Feb 16, 1993
Classifications
1
FEI Numbers
1106
Registration Numbers
1106
Same Product Code
57
Applicant Total
33
Review Days
42

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Basic Information

Device Name
CALMPS: BONE, MASTIN, LEWIN, BRAND
K Number
K930028
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thomasville Medical Assoc.
Date Received
January 5, 1993
Decision Date
February 16, 1993
Product Code
LXH
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
LXH Orthopedic Manual Surgical Instrument

Similar 510(k) Clearances

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

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Other Clearances by Thomasville Medical Assoc.

K Number Device Name
K926429 VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
K926531 HYSTERECTOMY FORCEPS
K926527 ROTO FIT BIOPSY FORCEPS
K926535 GOMCO CIRCUMCISION CLAMP
K926533 Z-CLAMP FORCEPS
K926540 SOPHER AND BIERER OVUM FORCEPS
K926532 ENDO CERVICAL CURETTE
K926536 DISPOSABLE PLASTIC VAGINAL SPECULA
K930030 SUCTION TUBES: HOUSE, BARON
K926484 CORSON MYOMA GRASPING FORCEPS
Search all 33 clearances from Thomasville Medical Assoc. →